EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS082-00505 
Organism
Homo sapiens 
Tissue/cell
HCASMC 
Coordinate
chr1:27829970-27832410 
TF binding sites/motifs
Number: 6             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
EWSR1-FLI1MA0149.1chr1:27830565-27830583GGAACGAAAGCAGGAAGA+6.13
Nfe2l2MA0150.2chr1:27831966-27831981TGCTAAGTCATTGTT-6.36
Nr2f6(var.2)MA0728.1chr1:27830156-27830171CGATCTCTTGACCTC-6
STAT1MA0137.3chr1:27831609-27831620TTTCCCAGAAA-6.02
STAT3MA0144.2chr1:27831609-27831620TTTCCCAGAAA-6.32
ZNF263MA0528.1chr1:27831218-27831239TGAGAATGGGGAGGAGGGAGG+6.04
Number of super-enhancer constituents: 30             
IDCoordinateTissue/cell
SE_02913chr1:27830213-27831026Bladder
SE_02913chr1:27831120-27832355Bladder
SE_05196chr1:27829210-27833352Brain_Cingulate_Gyrus
SE_05814chr1:27829181-27832931Brain_Hippocampus_Middle
SE_06945chr1:27829261-27832857Brain_Hippocampus_Middle_150
SE_07770chr1:27829738-27832662Brain_Inferior_Temporal_Lobe
SE_23188chr1:27830280-27832092Colon_Crypt_1
SE_24033chr1:27830527-27830952Colon_Crypt_2
SE_24033chr1:27830969-27832275Colon_Crypt_2
SE_24711chr1:27830217-27832142Colon_Crypt_3
SE_25901chr1:27830171-27832637Duodenum_Smooth_Muscle
SE_26518chr1:27830129-27832742Esophagus
SE_27625chr1:27830080-27832462Fetal_Intestine
SE_28547chr1:27830055-27832555Fetal_Intestine_Large
SE_29557chr1:27829444-27832772Fetal_Muscle
SE_31394chr1:27830159-27832397Gastric
SE_33477chr1:27830354-27831735H2171
SE_34755chr1:27830079-27832086HeLa
SE_35950chr1:27830256-27832335HMEC
SE_36974chr1:27829579-27833069HSMMtube
SE_39896chr1:27830278-27832548K562
SE_40593chr1:27829483-27832634Left_Ventricle
SE_42106chr1:27830105-27832560Lung
SE_48058chr1:27830093-27832593Psoas_Muscle
SE_48567chr1:27830115-27832554Right_Atrium
SE_50130chr1:27830153-27832341Sigmoid_Colon
SE_51091chr1:27829612-27832640Skeletal_Muscle
SE_52467chr1:27830150-27832427Small_Intestine
SE_62718chr1:27801410-27856116Tonsil
SE_65253chr1:27830186-27832347Pancreatic_islets
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr12783030427830805
chr12783080827832117
Number: 1             
IDChromosomeStartEnd
GH01I027502chr12782888927832715
Enhancer Sequence
TCTGTTGTCC AGGCTGGAAT GCAGTGGCGC GATCTCGGCT CACTGCAGTC TCCGCCTCCC 60
GGGTTCAAGC AATTCTCCTG CCTCAGCCTT CCAAGTAGCT GGGACTACAG GTGCGCACCA 120
CCACGCCTGG CTAATTTTTG TATTTTTAGT AGAGACGCGG TTTCACCATG TTGGCCAGGA 180
TGATCTCGAT CTCTTGACCT CGTGATCTGC CTGCCTCGGC CTCTCAGAGT GCTGGGATTA 240
CAGGCGTGAG CCACCGCGCC CAGCTCACTC TGAATATTTT GAGCGACCTA TTTATGATTT 300
GAATTTATTC ATTCGAGAAG CACCCCAACA TACCTCCTAT ATGTCAGGCA TGGACCCAGG 360
AACTGTGACT ACAACAGATA ATTAGGGGTT GGTTCCTCAG ACAGGACAAA GGGCAGGACA 420
CTGAGTGCCA CCTCTACAGA GGGGTCTGAC TGGATAAAGA CAAAGTGTGA AAGTGTATGA 480
CTTTCACAAA ACAAGAAAGC CAAGCCCCGT GTGGGGTGAC AGGGTGCAGG GATGGGAGAT 540
GGCACTCAGG GAGCTAGCAC TGGACAGGCC AGTGATTCCG AAGACAGAGG ATAAAGGAAC 600
GAAAGCAGGA AGAGAGGGAA TGAGTTATGG GTGAAATATT CGGATCCTGT AGCCTCCATA 660
GAAGGTGGCC AAGTGGGCAG GGGGCAAAGT CCCAGCCAAG CCCCTCAGCA CCCCCATGTG 720
TTCCCAGCCC TGCTGAGCCC TGCAGCTCGT CTCCTCCTGG CTCCAAAAGT CAGACCAAAC 780
CCCGGAGAAC AGAGGCGGGT GAGGAGGGGG CGGTGGGGTA CAAGCCCAGG CCTCTCACCC 840
CAGCAAAGCC TGCCTTCCCA GTGCCTGGGG CCAACCCAGC TGAGAAGCCA GAGGTTACAG 900
GGAAAGGATT AAGGAGTTGC TTGCTTTTTT ACCCAAACTC TGCTGTATTT CTCTGTCTTT 960
CTTCAATCTC TCTCTCTCTC TCTTTTTTTT TAAAGAAAAA TATTCCTGTA CACGCACCCA 1020
GAGGCTTTTG CAGGAGGCGG CTGTTGGAGA ACTGGGAAAA CAAGCCAAGA AACAAGAGAG 1080
AGGAAAAAGA CCACGCCTCG CCTGGCAGAT TCCTAATGGC CCAGGAGACC TGAGGCTTTA 1140
CAGTGGGAGG CCGGTGGGGG CTGGCTCGGG TGGGAGGGAA GGGCAGGCCG AAGGACAGCC 1200
ACTTGCTGGC TGGTGACCTT GGGCGGGATA CTGCCTGCTT CCCTCTGGTG AGAATGGGGA 1260
GGAGGGAGGC AGGGGCAGGC CTGGCCGGCT GAGGTCACAG GAAGGCCCCT TCCAGCCTGA 1320
AACGCGATCT CGGGATGTGG GGCCTGCCAA CCTGCAGCGA CCCTGGGCCA GCAGAGATGA 1380
AAGGCTGCCT GTCCCCAGCT TCCGGACCCC CAAGGCCCCA CTGCCTCAAA GTTGGAGAGC 1440
AGCAGAGCTG TGTTGCCACT GGCTGGGGCC AGCTGCTGGG CTCCCCACCC CACCTTATGT 1500
CATCCAACCC TCCCTTCCCT GTTTTGCAGA GGACACTCAG GCCCAGAGAG GGTGGTGACC 1560
TGCCTGAGGT CACACAGCAA GCGGGAGTCT GAGCCAAGGC TCACCACAGT CTTTGGACTC 1620
CAAGTCCAGG CCTCCTGCCT TTCCCAGAAA CTTGGCTGCC TGGGGGCTTA CCCTGGGGAG 1680
TTGGAGAGAA CTAGGGCTGG GGAGGACACT TAGGAGCTGT GTCTGTTTGA AGTCACAACT 1740
TAATGTTGAC TAAAGTGCTT TTTTTTTAAA AGACAAAAAG AAAATTCCCA GCCCCTGCCA 1800
TAAGCCTGGA CTTGCTCACT GGCAGGGGAA GGAATGCAGC TCTGGCCACC ACAGCTGCTG 1860
GTGGCCAGCT GCAGCCTCAG CTTCTGCTGC TCCCGCCCCA GCCGGCAAAG GGACAAAGGC 1920
CTCTTCTCAG GCCTGTCCTC TCCAGCCCCC TGGATCAGCT GGCAGAACAT TGACGGAGCC 1980
TCCTCTGTCA CAGACCTGCT AAGTCATTGT TCCTCTCTGG GCCTTAGTGC CGTTTCTGTA 2040
AAATGGGGGC ATAGTATCTG CCTGACCTAC TTCTCAGCAC TGTTTTGAGG CTCCAAGTAA 2100
AGTTCTGGAA ATACAAAGCT CTCAGCGCCT CCTTCCACCT GCGGGTCTGC CTTCTCACTG 2160
TGCCCTTTGC CTCGACCACC CCTCCCTCCC TCATGCTTTC CCTGGCCAGC CCCAACTCAC 2220
TCAGCTCAGC TCAGTGGGAC CATCACCTGC TCTAAAACCT GCCCTCAACT TCTGAAGGAG 2280
GCACCTTCAG AAGAAAAAAG ACGGCAGTGC TGTATTTATC ATGGTTGTAC ATAATTAAAT 2340
AATTGGCCAG TGTGGTGCCT CAGGCCTGTA ATCCCAACAC TTTGGGAGGC TGAGGTGGGA 2400
GGATTACTTG AAGCCAGGTG TTCAAGACCA GCCTGGGCAA 2440