EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species

TagContent
EnhancerAtlas ID
HS116-00144 
Organism
Homo sapiens 
Tissue/cell
Left_ventricle 
Coordinate
chr1:8430040-8435250 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs3795310chr18431607hg19
TF binding sites/motifs
Number: 4             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
HOXC11MA0651.1chr1:8432711-8432722GTTTTACGACC-6.14
MNX1MA0707.1chr1:8433964-8433974GGTAATTAAA+6.02
RREB1MA0073.1chr1:8434924-8434944CCCCATACCACCCCCACCTC+6.58
ZNF263MA0528.1chr1:8434930-8434951ACCACCCCCACCTCCTCCTCT-6.11
Number of super-enhancer constituents: 29             
IDCoordinateTissue/cell
SE_00045chr1:8428649-8443854Adipose_Nuclei
SE_01103chr1:8430093-8435200Adrenal_Gland
SE_02100chr1:8430087-8435260Aorta
SE_03407chr1:8430125-8433201Brain_Angular_Gyrus
SE_03407chr1:8433769-8434446Brain_Angular_Gyrus
SE_03947chr1:8429979-8435152Brain_Anterior_Caudate
SE_04978chr1:8429969-8435444Brain_Cingulate_Gyrus
SE_06073chr1:8429716-8435428Brain_Hippocampus_Middle
SE_07042chr1:8429911-8435349Brain_Hippocampus_Middle_150
SE_07921chr1:8429992-8435571Brain_Inferior_Temporal_Lobe
SE_11329chr1:8433034-8440258CD20
SE_18764chr1:8432600-8435408CD4p_CD25-_Il17-_PMAstim_Th
SE_25808chr1:8429703-8435722Duodenum_Smooth_Muscle
SE_30827chr1:8429997-8435596Fetal_Muscle
SE_31622chr1:8431308-8432140Gastric
SE_31622chr1:8432260-8433382Gastric
SE_31622chr1:8433410-8435297Gastric
SE_37218chr1:8429830-8435291HSMMtube
SE_40658chr1:8421188-8437093Left_Ventricle
SE_42166chr1:8430032-8435460Lung
SE_45677chr1:8429996-8435732Osteoblasts
SE_47251chr1:8431698-8435541Panc1
SE_48103chr1:8430035-8435429Psoas_Muscle
SE_48600chr1:8430022-8435331Right_Atrium
SE_51176chr1:8429583-8435786Skeletal_Muscle
SE_53408chr1:8430412-8435294Spleen
SE_54819chr1:8429674-8441643Stomach_Smooth_Muscle
SE_63725chr1:8430031-8431274HSMM
SE_63725chr1:8432400-8434994HSMM
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 8             
ChromosomeStartEnd
chr184302218430306
chr184304178431722
chr184326318433251
chr184332898434374
chr184320798432211
chr184326008432949
chr184335948434372
chr184349748435178
Number: 1             
IDChromosomeStartEnd
GH01I008369chr184296818436259
Enhancer Sequence
GGGGTTTCAC TGTGTTTGCC AGGATGGTCT CGATCTCCTG ACCTCGTTAT TTGCCTGCCT 60
CGGCCTCCCA AAGTGCTGGG ATTACAGGTG TGAGCCACCG TGCCCAGCCA GAAACTATTC 120
TTAACAGTCC AAACTGGAAA CAACCTAAAT GCCCACAAGC AGGAGAATGG ATAAACAAAT 180
AATGGTATCC CCACATTCAC TGGACTACAA CTTGGCAATT AAAAGGCACA GACCACCGAC 240
ACATGCAGCA ACACCATGCT GCATGAAAGC AGGCAGACAG GGACGGTGGG TGCTGCGTGA 300
GTCCTTCCCA GAGATCACAA AAACCAAACT AGCGGTTGCC GAGAGCCTGG AGGGTGGGGG 360
ACAAGAAACT AAAAGAACTC AGGTAAGCAC TCCAGGGTGA TGAAAATGCT CTGTAAGTTG 420
AATGTGGTGT CACTGACACA AATGTATACA GTGGTCAAAA CTCATGAAAC TGTGTACTTA 480
AAGTGGGTGC ATTTTTACGG TATTCATACC ATATATGGCA GGTTACGTCA ATAAAGCTGA 540
AGAAAAACAA CAACAAATCC AGGCCGGGTT TTATTAGCTG CCTCTCAACC ACTGTTATGC 600
CTATCAAGGG ATTCAACACT GGAATGAAGC GAGTCTAGGA TCGGAAATGG CATATTGGTG 660
ACTGCATGGG TGGCAAGGTC TTGAGCACAA ACAAAAGAAC ATGTCGGGGA AAGCTCTGGT 720
TCTACAAATA GGGAGTGAAG CAGCTAGAGG CCTCGCCAGG AATGAAGTCA ATTGAACTTT 780
AATCAAACAT GCATAGTGTG TGCTGCAGAG ACCCGCTGCA CATAAATTCA GGGAACAAAA 840
GCTGTTGCAG AAATCAATAG CTTACTGAAA CATTAACACA GGCAATCATT AATCAAAAGG 900
CAGCTCCACA AAGGCAGCCT TGCAAATTAG CTCCTGATTT TGCCTGCAAG CAAACACAGA 960
GGTATAAAAT GTTGTCGACA TGAATGGCCT ATAATGATCA TTTTGCTCCT GATGCTCTCA 1020
CCTCATCTCA CAACAAGGTC TCACAGTCAA CATATCTTAT GTCTCGGTGC TATAATTGCA 1080
CACAGCATGA GGAACTCAAC TGGTTTAGTG CCTGGGCAGA AATGGGAAAG GAAGAGGGCG 1140
AAGTCATCTC CAACTGACAG TGTTCCCGGC TGCAGCTCTT GCCAAGAGAA GTGCTCAAAT 1200
CCATTGGGCT ATATTTAGCA GATTCTCTCT CCTTTCCTTT TTCTTTTGGC GGTGGGGGGG 1260
CTAAATTTTT CCCACAGGTC ATATGCAAAA AGCCTTTGGC AATGACAGGA GCTTGGCTCC 1320
TGGACTTAGG AGTCTCTTCC CAGCAGAGGT GTCTTTCCAG GCTATACACT AAGATGGAGT 1380
TAGGAAAATA AGCACCATTA GGTTCCTTTA ATTTCCCACA AAAAGAAAAA CAAGGGGAAG 1440
GGAGTGCCAC ACATGGAAGA GAGAGGGAAG AAGTAGTAAG CTGCTTGGCA CCAGGCAATC 1500
TGGGTGAAGG GCCTTAGGAG AGAAGGAAAA AGCTAAGGAT GCAGAGTCAG CTGACTCTGG 1560
GCCTAGCGGA GGGACAGCTC AGCGGCAGCC GCTCCTGCCA TCCAGGGGCC TGCTGGGCTC 1620
AGGCCACTTT CTCCTCCTCA GCCACCACTT TATTTCTGCC CCCTCCAGGG TTAGGCTGCA 1680
AGTCTATCAA GTTCACACAG ACACAACGTA AGACATCAGC ACAGGTCTTT AAGAGCTCCC 1740
TCCGCCGCCT GGGCAATCTG GGCTGGAGCA ACAGGGGCCG GGGCTGCCTA CCTCCTAGAG 1800
GCTGCCTGTA CCCATTTCAG GTATTAATAC TGGTTCTGCT GTTCTGGCCA GGCCCAGTTC 1860
TGCTTTATCT TGGGTAAGTG ATAGGCAACC CGACCCAGGG GCCAAGTGGG TGCCCCTGTG 1920
TATGTGCATG TGTGCACAGA TGTGAGCAGG GTCTCCTCCC AGGCTTTCCA ACAGGCCAAC 1980
TTACCTGTGC GCATTTGGTA AACTAAACAC TATCCACCAA CACAACTGCT ATTTAATTTC 2040
CCACAGGCAG TGGAATGCTA CGGGAAGAGA ACCTGTAACC TGTCCTGTGA TAAGCCACAT 2100
GTCTTCTCTC TCTTTAGGGG CATGGGGGAG TGAAAGAGTA GAAGAGATTG TTGAAGAAGA 2160
AGGCACTGGA AGCATTTTGA CTATAAAAGG CTCACTCGTA GCAAGCATGC CTGTTTCAAA 2220
CAGTATGGGG CCCAGCTTCT CTTCTGCCCG AGCCCAGCAT GAACTGCTCA GACAGGATCC 2280
TCTGAGAAGC TGACATGGAG GCAGGAGAAG GTTAAATCAA TGGTTTCTGC TGTCCCATAT 2340
TAGAAGCATA AGGGTACACC CAAGATTGAG TCCCACTTTT TTTGGTAATT ATATCATTAT 2400
TACCACATCA CCCAAGAAGT CTGGACACTC CCCTGAGGAA GGGGAGGGAG TGCAATAGAA 2460
GATGAGGTCT GGAGACTCCC ACACACGGTA TCCAGGGTGT CTGCAGCCTG CCACCTACCA 2520
TCAGGTCGTG TGTGTGTGTG TGTGTGTGTG TGTGTGTGTG TGTTTTAAAT TAAGCCAAAG 2580
AAGGACTCAG TCCTTTGTAA ATAACCGTAT GCGCACCCCC TTTCGATTCA GTTCACAGAG 2640
AACAGTGAGA ATCTTCCACT GTCACAACAC AGTTTTACGA CCAACAGCAA AGAATGATGA 2700
GGACTGCTGG CCTTACGGCT ATGTTAAGGA AGGCCCTGGA ACACCAGTTT CCTGCCTCCT 2760
TGCCCATGCA GACAGAGGGG AGATACAGGC AGGCAGGCAT CTAAACCAGA TCCCTGCAAC 2820
GTCACATATG CCCAGGCTCT GGCCTTGTGC CACTAGTGAG GGTCAGCTGC AGCTCCTTTC 2880
TTTTTCACAA ACGAAGTTTC CAATGGGCAC CCTTTCTGGG CCATGCATCG CCCACTAAAA 2940
AGGAGGGGGC AGTCGGAGAG AAGGGGGATG AGGAGGCAGG CCTGGAAGCT TCTCATGGAT 3000
AACAGGATTA TAAACACAAT TTCTTTCCGA AGCTATTTCA CAGGTCTTCG AAGCCCACCT 3060
ACCACTGTCA GCTGAGCAGA CTGTAGTTAC GTGATGGGAC AGGAGCCAAC AGGGGCAGGG 3120
CTGCTGAGTG CACATCCTTG TACGCACCTG ACCCCATCGC AGAGTCTTAG AAGTAAGCAT 3180
TTAGAAGAAA TCATTTTAAT TCTTTAAGAC ACAAGATTAT CTGTTCCTAT GGCTAAACAA 3240
ATATTTTAAC ATGAATACAG AAGGAGCAGC TAAATAATCT CTACACAATG CCTTAACTCT 3300
CGGTGCTAAT GTGCAATTAG AGTCAGAATG TTGTTCCCCT GCTTAAACTT TTGTTTGAAA 3360
AAATGCCCCA CAGTGAGCAT CTGGCTCCTT CTTTGGTGGT CCACGTAAAG GGGATGAAGA 3420
AATCCACCCC TTCCTTACTG AAGTGGAGAG ATCTAAAACT TTTTTTTAAG GTATGTTTTT 3480
TCAGGGAGAA ATCCCAGCAA GCAACAAATA ATAAAAAACA AGGCCTCAAA TTATGTAGGG 3540
CAGAGAGGGA GAAAGAAGCA TGGTGTAGAG CTGCTTCCTA AACCCGGGCC CAGAGAGTGA 3600
CCCAGGCCAT GAGGAAAGAG CTGTGGCCCT GAGAGCCGGT CCCAGGAAGT CTGCATGCGA 3660
CGCTGTCCCC TGAAGAGCTG CCCTAACTGG AGTGCTCCAA CGCTGCTGCC GAGTGCAGTC 3720
AGGAACATTT CCTGGCATGG AATCCTATGC GAGTCATTCT TTCCTTTCCC TCCCCAACGA 3780
TTCAAGGGCT GGATCTGACA ACTGTTCAGA ACATCTGAGG TGAGAAGCCG GGCACTGGGC 3840
AGAACCAGCA GCGATATTCA GGAGCAGCCA CCTTCTACAG ATCTTTTTCC AGGAGGCAAC 3900
CGGTTGTCTT CCAGTAACAA CTCTGGTAAT TAAAGCACTG TTCTCCTGGG CTCCTTCTTT 3960
TGTTAACCAA CCGAATCCTC TAATCCCTAA AGGAGCCTGG CACTGTCAGC GGGCTCTGCT 4020
GCTAATCGTT AAATATCACC TCTGTGGTCT CTGAGTGCAG CAGGGAGAAT GATGATCTGC 4080
TTGAAGGCAC ACGCAGAGAA GTGGAATTCT GAAATCTCAG CCTCCTACGT TCAAGAGGCC 4140
GAAGGGCTCT GATCTAAACC GCCACCCACG AGGAAGCCCA CAGTGAGGAG GCAGCTGCCT 4200
CCAGGCAAGG CAGTCCCTCG GTGCCACCTC CAGATCCTCT TCTGGGGAAA GGCAAAGGGA 4260
AAGGAGGGAA GTACGTGAAG GTCTTGTGGC TTTAACTTGT AAATAGGTGG GGCCAGTCTA 4320
AGACACTCAT GAAGATGTTC CTTACCCAGG CACCTTTTTA TAACATTTTA AAAAATCAGT 4380
TAAAAAAAAT TTTTTTTTTA CCACTACATT TACCACTCCA TTTGTACAGT GCAAAGGAAC 4440
TGCAATAGCT CAAGATTTCT GCCAACACTG AACACTGTAA TGAGATTTCC TAAGCTCTGT 4500
GTTGTTCTGG TGGATGAACT CAGCCATTTG CTAATCCCAC CCTGGCCCCA CACCTCCACT 4560
CAGACGTCTG GACCTGAGGT CCTGCCACAG CTCTTCCCTG GGCCGGCCCT CCCATGCTGC 4620
ACACAGACCA GGTGAGTCTT CCCAAAGCCC CGCTAGTACC TTGCCACTTC TTCTCCAAAC 4680
GGTCAAAGGT TCCTCAGGGC CTAAGGAACA AAGGCCCAGC TGCTTGACTA CTTCTTCTGA 4740
GACTTTCTCT GTGTTACCGG AAGACTTTTC TACCATATTC CTTTCTACCA TATTCCCCCG 4800
CCTCACGGCC TTTGGCTTAT GTCAAACACA ATGGCCAGTT TTCTGTTCCT CAGCACTCTC 4860
CTGCCTGCTG GGTGAGCCCC TGAGCCCCAT ACCACCCCCA CCTCCTCCTC TGTCCAGGCC 4920
CTGTAGTCCT CCTCATCACT CAGGACTCAA TTCATCACAT TTGCTGCCTT CTTCTCCATG 4980
AAGCCTTCCC TTCACTTCAC TCCCCCACCA CTGGATGGCA TCATACAGGT TTCACTCCTA 5040
CATCTTTTCA TTCCCGCCTC TGTGCTGGCA CAGACAGGCT TCCCTGTGCT GTAACCATAC 5100
ATGGGCCCAC CCAACTTGCC AAAGTACGTG CTATCTCATC TGTGAGTACC CCACAGGTCT 5160
AAGACAACAT CTTGAATAAG TATTCAGTAA ACATCTGATG AAATGATTAT 5210