EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS062-15214 
Organism
Homo sapiens 
Tissue/cell
GM18486 
Coordinate
chr7:102028880-102031800 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs117530689chr7102030935hg19
TF binding sites/motifs
Number: 21             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
CTCFMA0139.1chr7:102031358-102031377TGCTGCCCTCTGGTGGCAG-7.87
EWSR1-FLI1MA0149.1chr7:102029460-102029478GGAGGGAGGGAGGGAGGG+6.03
EWSR1-FLI1MA0149.1chr7:102029464-102029482GGAGGGAGGGAGGGAGGG+6.03
EWSR1-FLI1MA0149.1chr7:102029439-102029457AGAAGGTAGGAAGGGAGG+6.52
EWSR1-FLI1MA0149.1chr7:102029431-102029449AGAAGGAAAGAAGGTAGG+6.65
EWSR1-FLI1MA0149.1chr7:102029451-102029469GGGAGGAAGGGAGGGAGG+6.92
EWSR1-FLI1MA0149.1chr7:102029455-102029473GGAAGGGAGGGAGGGAGG+7.08
EWSR1-FLI1MA0149.1chr7:102029435-102029453GGAAAGAAGGTAGGAAGG+7.94
EWSR1-FLI1MA0149.1chr7:102029447-102029465GGAAGGGAGGAAGGGAGG+8.06
EWSR1-FLI1MA0149.1chr7:102029443-102029461GGTAGGAAGGGAGGAAGG+8.08
IRF1MA0050.2chr7:102029733-102029754TTTTTCTTTTTCTTTTTTTTT+6.09
Pou2f3MA0627.1chr7:102030462-102030478TTGTATTTGCATACAG-6.35
STAT1MA0137.3chr7:102030727-102030738TTTCTGGGAAA+6.02
STAT3MA0144.2chr7:102030727-102030738TTTCTGGGAAA+6.32
ZNF263MA0528.1chr7:102029453-102029474GAGGAAGGGAGGGAGGGAGGG+6.54
ZNF263MA0528.1chr7:102029465-102029486GAGGGAGGGAGGGAGGGGAAA+7.02
ZNF263MA0528.1chr7:102029457-102029478AAGGGAGGGAGGGAGGGAGGG+7.05
ZNF263MA0528.1chr7:102029449-102029470AAGGGAGGAAGGGAGGGAGGG+7.27
ZNF263MA0528.1chr7:102029461-102029482GAGGGAGGGAGGGAGGGAGGG+7.97
ZNF263MA0528.1chr7:102029452-102029473GGAGGAAGGGAGGGAGGGAGG+7.9
ZfxMA0146.2chr7:102029985-102029999CCCGCCTCGGCCTC+6.01
Number of super-enhancer constituents: 1             
IDCoordinateTissue/cell
SE_60478chr7:102022497-102092339DHL6
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr7102031086102031660
chr7102030200102030800
Number: 1             
IDChromosomeStartEnd
GH07I102390chr7102031261102031450
Enhancer Sequence
GGTGGTGCGT GCCTGTAGTC CCAGCTACTC GGGAAGCTGA GATGGGAGGA TTGCTTGAGG 60
CTGAGAGGCA GAAGTTACAG TGAGCAGAGA TCGAGACACT GCACTCCAGT GTGGGCGACA 120
GAGTGAAACT CTGTCTATGA ATAAATAAAT AGAAGTATAT GGTTAAATAA GTTTGATAAA 180
TGTGGATGGT TGTGTAGCTG CCACCACAAT TCAGATATAG AACATTTTTG TCATCCAAAT 240
ATTATGCAGA GAGGCCAGGT GCAGTGGATC ATGCCTATAA TCCCAGTGCT TTGGGATTCT 300
GGGGATAGAA GGATCACTGG AAGCCAGGAG TTTGAGACCA GCCTGGGCAA TACAGCAAGA 360
CATCATCTCT ACAAAAATAA TAATAATAAT AAAGTAAAAA TAGCCAGGTG TGGTGGTGTG 420
CACCAATAGT CCCAGCTATT CAGGAGGCTG TGGCAGGAGG ATCACTGAAG CCCAGGAGTT 480
TGAGGCTGCA ATGGGCTATG GTCACGCCAC TGCGCTCCAG TCTAGGCAAC AGAGTGAGAC 540
ACCATCTCAA AAGAAGGAAA GAAGGTAGGA AGGGAGGAAG GGAGGGAGGG AGGGAGGGAG 600
GGGAAAAAAT ATCTATTACC CAAGAAAGTT CCCTGAGGCC CTCCCAGGTC AGTCCCGTCC 660
TCCTACTTGG CCCATGGCAA CTGCTGATCT GTTTTCCATC CCTATCATTT TGGCTTTTCC 720
AGAACATCAA GTAAATGGAA CCATTCAGGT TGTGGCCTTC TATTAATAGA TCTGACTTCA 780
CTCACTAAAC ATAATGCATC TGAGATCCAT CCACGTTATT GCAAGCCTCA AGAGGTCCTT 840
CCTTCCTTTT TCTTTTTTCT TTTTCTTTTT TTTTTTTTTG AGATGGAGTC TCACTCTGTC 900
GCCCAGGCTG GAGTGCAGTG GCACGAGCTC GGCTCACTGC AAGCTCCGCC TCCCGGGTTC 960
ACGCCATTCT CCTGCCTCAG CCTCCTGAAT AGCTGGGACT ATTGGTGCAC ACCACCACAC 1020
CTGGCTAATT TTTTTGTATT TTTAGTAGAG ACTGGGTTTC ACCCTGTTAG CCAGGATGGT 1080
CTTGATCTCC TGACCTCGTG ATCTGCCCGC CTCGGCCTCC AAAAGTGCTG GGATTACAGG 1140
CATGAGCCAC CACACCTGGT CCCCTTTTTT TTTGAGATGG GGTCTCACTG TCGCCCAGGC 1200
TGAGTGCAGT GGTATGATAT CTTAATCCAC CTTCTTAATC CGACTCACTG CAACCTCCGC 1260
CTCCTGGGTT CAAGCAATCC TCCTGCCTCA GCCTTCCAAG TACCTGAGAT TACAGGTGCA 1320
CACCACCATG CCCAGCTAAT TTTTGTATTT TTAGTAGAGA TAGGCTTTCA TCTTGTTGGC 1380
CAGGCTGGTC TTGAACTCCC GGCCTCAAGT GATCCTCCCT CTTCAGCCTC CTAAAGTGCT 1440
GGGATTACAG TCATGAGCCA CCGCACTCAG CAAAAGCTCC TTCCTTTTAT TGCTAAGTAG 1500
TATTTCCCTG TAGGTCTAGA TCTCAATTTG ATGGACATAT GGGTTGTTTC CAGTTTTTGG 1560
CAATTATGAA TCAAGCTACT GTTTGTATTT GCATACAGGT CAGTCAGTGG ACATATATTT 1620
TCATTTCTCT AGTTTGAGAC CAGCCTGGGT AACGAGAGTG AAACTCTGTC TCAAAAAAAA 1680
AAAGAAAAGA AAAGAAAAAA AGAAAAAAGA AAAAAAACCC TGCTGTTTTA GTACTTAAAG 1740
TATCAACCAC TACTCAAAGA ATTGAGATAG GAGTACCCAC TCGTCTAGGG TAATCAACCA 1800
TCCTGGCTTG CCCAAGATTC TCCTGGTTTT AGCACTGAAG GTCCCACTTT CTGGGAAACC 1860
CTTCAGTCCT AGGATCAAAC TAGGACAAGT GTGGTCACCT ATTTTTTTTT TTTTTTTTCA 1920
GACAGAGTCT CTCTCTGTCT CCCAGGCTGG AGTGCAGAGG TGCGATTTTG GCTCAGTACA 1980
GCCTCCGCCT CCTGGGCTCA AGCAATTCTC CTGCCTCAGC CTCCCGAGTA GGTGGGATTA 2040
CAGGCAGCTC CCCCCACCCC ACACGCCCGG CTAATTTTTT TTGTATTTTT AGTAGAGACG 2100
GAGTTTCACC ATGTTGGCCA GGCTGGTCTC GAACTCCTGA CCTCAGATCA TCCACCTGCC 2160
TCAGCCTCCC AAAGTGCTGG TATTACAGGC GTGAGCCATG TTATTGAATG TCAGGCTCTG 2220
CTGGACACTG CATGTCCAAA CGTCATTTTA CCCATGTGCC AGCGACAAGG TAGATTCGCT 2280
TGTACCAATT TTGCACATAA GGAAACAGCC TTAGAGAGGT TAGGTTGCTT GTGCAAGCCC 2340
AGGGTAGGTG GCACCCAGTC TGCCAGTCTG CAACGCACTG GTATCTTCCA GCCAGTAGAC 2400
CTTGCTCCCT GGGTGCCCAG TTCTGGATCT CAGGAAAGGT GGATTAAGGC TCCTAGTGGC 2460
GGGACCTGGG TGGGGATTTG CTGCCCTCTG GTGGCAGAAG GGACATCACC CTGGGTGTGA 2520
GACTTGTGGG CATCTGTGAG GCGGCCTTTC ATCCCAGGGA GCCGGACCTC AAATCTGACC 2580
TCAGCCCCAG GAAGGTGCCA CCAGGAAGGT GCCACCTAGG AGGGTGCCAC CAGGGTTCCC 2640
GCCAGGGTCT GCTGGGGCCC TGTCCCATCT GTGTGAGTCA CATAATCACT CAGGCTGTCA 2700
CAGACCCAGG GCTAGACTGC TGGGTTTGAG TCTGTGTGGC CCTGAGCCAA TTGCTTTCTC 2760
CTCTGGGCCT CAGTTCCATT TCAGTAGAAT CAGGATGATA GCCTGGGCAA CATAGCAAGA 2820
CTCCAGCTCT ACCAAATAAA TAAATAAATA AATAAATAAA TAAATAAATA AATAAAATAT 2880
TAGGCTGGGC AAGGTGGCTC ACGCCTGTAA TCCCAGCACT 2920