EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS003-00571 
Organism
Homo sapiens 
Tissue/cell
A549 
Coordinate
chr1:21948910-21952090 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs1318236chr121952024hg19
TF binding sites/motifs
Number: 17             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
EWSR1-FLI1MA0149.1chr1:21950675-21950693GGGAGGAGGGAAGGAGGG+7.36
HNF1AMA0046.2chr1:21950208-21950223TTTTAATAATTAACA+6.05
HNF1BMA0153.2chr1:21950209-21950222TTTAATAATTAAC-6.14
KLF16MA0741.1chr1:21949073-21949084GGGGGCGGGGC-6.02
KLF16MA0741.1chr1:21949134-21949145GCCACGCCCCC+6.62
KLF5MA0599.1chr1:21949074-21949084GGGGCGGGGC-6.02
KLF5MA0599.1chr1:21949107-21949117GGGGCGGGGC-6.02
KLF5MA0599.1chr1:21949112-21949122GGGGCGGGGC-6.02
NRF1MA0506.1chr1:21949176-21949187GCGCCTGCGCG+6.14
SP1MA0079.4chr1:21949131-21949146GAAGCCACGCCCCCC+7.49
SP3MA0746.2chr1:21949133-21949146AGCCACGCCCCCC+6.74
SP4MA0685.1chr1:21949131-21949148GAAGCCACGCCCCCCGG+6.42
SP8MA0747.1chr1:21949134-21949146GCCACGCCCCCC+6.44
ZNF263MA0528.1chr1:21949557-21949578TTCCTCCTCCTCTCCTCCATC-6.05
ZNF263MA0528.1chr1:21949554-21949575CTTTTCCTCCTCCTCTCCTCC-6.16
ZNF263MA0528.1chr1:21949549-21949570TGTCCCTTTTCCTCCTCCTCT-6.65
ZNF263MA0528.1chr1:21949564-21949585TCCTCTCCTCCATCCTGCTTC-6.73
Number of super-enhancer constituents: 11             
IDCoordinateTissue/cell
SE_00987chr1:21949130-21950367Adrenal_Gland
SE_00987chr1:21950822-21951982Adrenal_Gland
SE_04282chr1:21949177-21952719Brain_Anterior_Caudate
SE_05416chr1:21949072-21952361Brain_Cingulate_Gyrus
SE_06618chr1:21949350-21952242Brain_Hippocampus_Middle
SE_08200chr1:21949387-21953199Brain_Inferior_Temporal_Lobe
SE_31655chr1:21944407-21954108Gastric
SE_41934chr1:21949180-21952051LNCaP
SE_47603chr1:21949067-21950213Pancreas
SE_47603chr1:21950289-21952007Pancreas
SE_65280chr1:21949125-21951967Pancreatic_islets
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr12194920021950637
Enhancer Sequence
AGCGCGGCCC GGCCCGGCCC CCGCCGGGGC GGCACTTCAG CTGGCCCAGC CGGCTCCTGG 60
CCCGCGCGCG CCCGGGTCCG GGCCCCGCAG CGCTGAGCTC CGCGCTCCCG GCTCCCGGCG 120
GCGGCGCTGC CTGCGATGGG CTCGCCCCAC GGCGGGGCCC GGAGGGGGCG GGGCGCCAGG 180
TACGGGCGGC ACGGCGCGGG GCGGGGCGGG GCGGGGGCGC TGAAGCCACG CCCCCCGGGC 240
GGCCCGGCCC GCGGCCCCGG GACACCGCGC CTGCGCGTTC CGGCCCGAGC GCTAGAAGCT 300
TTGGGTGCGT CGGGCTCCCC GAGGGGGCCC CCCACTCGGT TCTCCCCAGC GCGCCCCCAC 360
CTCACTTTCT CCATCTTCCC AGGCTCTGGG TACCCCGCCT CGGCATCAAG GACAGGGTTG 420
GGTTACCTTG CAGACAGAGG GCTTTTCTTG AGCACCTACT TAATGCTGGG CCCTTCGCAT 480
GTGTCGTAAT CTCGTCACAG CCCAGGAGGT ACAAATGTCA TCTCCATTAT ACAGATGAGA 540
AGCCGGTTCC AAGAGGTGAA ATAGCTTGCC CGAGACCACA CAGTCAGGAA GAAGTCAAAG 600
TGGAATCCAG AGAAAGGCCT GGTGCTACTC TTTGGGGTCT GTCCCTTTTC CTCCTCCTCT 660
CCTCCATCCT GCTTCCCATG CCTCACAGTG GCTGGCCTGC TCCGTCCCTT CCCCCGCCCT 720
AGCTGCCCCA GATCCTGGGG GAGATGGCCA CAGCACCTAG GGAGGGGCTG CCAGGCCCGT 780
GGTATGGAGG AAAGGACCCA AGTAGATTTT GGGACATGTG GATTCTAGCT ACAACTTGCT 840
GAGTGGCCTT GAGTGAGTCC CTGCCTCCTC TCTGGACCTC AGTTTCCCCA TCTTTAAAAT 900
ATAAGGACTC TGTAGGCCCT TCCAGCTGGC TCTGCAGTGT GTCCCTGGCC TGGTATAGCC 960
ACTGTACAGC AGGGACAGGG ACAGGGCCTT GCTACCACTT CCTCCAGACA GATGTTGGGA 1020
ACACAGCAAA TGCTTCCTGA ACTGTGGCCA AGCAGACACA GCTGCTTTGG ATGTTGCGGG 1080
GGCAGGGCTG CCCACCAGCT CAGAGCCATA CCTCTGTTCA GCTTCCTGAA AGAGCTGCCA 1140
GTGGCTGCCC ACCACCCTCC AGCCCCAGAA CTAAGGGCTC CTGGAAGGAA AGCACTGTGC 1200
CCTCCCTTTC CCCCTAGACC TGGCCTTGAA TCAGGTTTGG GCCTGGAGAG CCAGCAGGAA 1260
CTCTGGAGAT GGGTGTTCCA GACACGGTGT AGCTTTGGTT TTAATAATTA ACAACAGCAA 1320
ATATTGATTT ATGCAGCCAC TTCCAGGCCT GAATGCTTCC GGGCACCCAT CGAAATCCAG 1380
CCAGAGAAAC ATCCATTCCC ACACTGCCCC CGGGGGAGGC GAGACCTGCT CACAGCACTG 1440
GAGATGGCTG TGTGCCAGGT GGCATGGAAG GTGTGTGCAC ATATGCGTGC AGCCATGTGT 1500
GCGTGTGTGT GAGACTCCAC GACCGGATGT GGCTGTATGT ATGTGGGCAT ACTGTCTTTC 1560
TGTGTGTATG GGAATGCCTT GGTATGGGAA TTTGTGTTTG TACATGTGTA TCTCATGCAT 1620
GTGCAAGTCT CTGAATATAT TTACAGACCA GTGGCTGTGG CTGTGTGTTT TGTGTCTGTG 1680
ACTCTGTCCC CATATGTAGG TGTGGGTAGG CTGTGTATGT ACGTGTGTGC AGGTTTCTGA 1740
ATCCCCGAGT GGAGAAACCC CTGTAGGGAG GAGGGAAGGA GGGTCCTGGG TAGCTCGATG 1800
CCTGTACAAA TGTGGGGCCT GAAGGGAGGA GAATGTCCCT TCTGGGTGCC CTGTCCAGCC 1860
CTGGGAATGT AATGACGCTG ATAAGAGCTC AGCTTCCTAA TTTCTACTTT CCAAAGTACT 1920
TTCACCCAAT TGCAAGCTGG CAAGGCAGGT AGAGAAGAAA CTGTCACCTC TGTTTTACAG 1980
ATGAGGAACC TGAGGCCCAG AGACGGGCAG GGATTTGCCC ACTGGCAGAG GAAGGTCACC 2040
TGCCCTTCAG ATGGATGCCA TCCATGTTAT AAATGTGCAC AGAGCTAGGG GCACCAGGGG 2100
AGGGGAATGG AGAATATGTC ACAGGCCTGT GTTCCCTCAG CCCAGCACTG GCTTGCTGGA 2160
GACCCCAGAT GAATCATTCA GTCTCTCTAG CCCCTGGTTT CCTCTCCTGT CAAAGGAGGA 2220
TGGTCCACAG ACTCTTGATT CTGAGGTGGG GGTGGGCTGT CGGGAAGGGA AGGTTCAGAG 2280
CCCGCTGTCT GAGCTGTGTT GGCACAAACG GAGGCTTCTA GCCAGACTGG GTGGAAGCCA 2340
GGAAGCCCGA GGGGAGGCAG CTTTTCAATA ATCCGAGAAG GCCAACCCCA GGCTGTCTAG 2400
CACGCAGGGC CCAGGGCTAT GGGCTGCTCT CTCTCTCTCT CGTCTCCTGA TGGGAAGACT 2460
GAGGCCCAGG GAGGGGAAGC TGTGGTCCGA GGGCATACAG CCCTTGGTGA GAACCCAGGG 2520
CTCCTCCTGA GATGCTCAGG GGAAGAGGGA CTGGGAGCTT CATTCATGAA CCCAGCTGTC 2580
AAGTGAGGGC TGCCATTGAG TCTCTCCCTT CCTGCCAAGC CCCGGATCCA CATGCCCCAG 2640
TCTTGGGCTG TTGCCCAGAC AGAGAAAACA GGAGTCAGTC TCAGGAATCT CCTGCTGCTG 2700
CTCCCAGCAG CCCCACGTGG CACCCCCATG AAGGTGGTGG CCCCACATAT GGACACCATT 2760
CCTTGGCCAT CTGCCCTCCC AGCCTAGGCA AGGTACGTGG CCTTTATTCC AGGCCAGAGC 2820
TCTCAGGGAG GAGCCTGGTG GATTTTGCCT CTGCTATTTT CTGGCTGTGT GACCTTGGGA 2880
AGACCACTTT ACTTCTCTGA TCTCCTGCAT CCTCAACTAG ATAATGCCTA CTACCCAAGG 2940
TTTACTAAAA GGACCAGGTG GCATGATGTC TGTGGGTGTG CTTTAGAAAC TGCAAAAAGT 3000
ACTGCAAAAG TGAGAGCTTG TCACCCCTGC ATCAGAGAGG CCCTAACACC AGGCCCTCTG 3060
GTCAGACAGC TTGCATCCGG TCGTGGCCCC ACCACATCCA ACCTGAGTGA CTTCGGGCAA 3120
GTGACTGAAC CTCTCTGAGC CTCAATTTTC TCATCTGCAA AATGGGACTG ATTATAGTAG 3180