EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS184-06888 
Organism
Homo sapiens 
Tissue/cell
T47D 
Coordinate
chr11:126015840-126018390 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs111977000chr11126017059hg19
TF binding sites/motifs
Number: 30             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
EWSR1-FLI1MA0149.1chr11:126017058-126017076CCCTCCCTCCCTCCCTCC-6.03
EWSR1-FLI1MA0149.1chr11:126017062-126017080CCCTCCCTCCCTCCCTCC-6.03
EWSR1-FLI1MA0149.1chr11:126017099-126017117CCCTCCCTCCCTCCCTCC-6.03
EWSR1-FLI1MA0149.1chr11:126017088-126017106CCTGTCTTCCTCCCTCCC-6.04
EWSR1-FLI1MA0149.1chr11:126017092-126017110TCTTCCTCCCTCCCTCCC-6.36
EWSR1-FLI1MA0149.1chr11:126017084-126017102CTTTCCTGTCTTCCTCCC-6.38
EWSR1-FLI1MA0149.1chr11:126017122-126017140CTTTCCTCCCTCCCTCCC-6.42
EWSR1-FLI1MA0149.1chr11:126017117-126017135CCTTCCTTTCCTCCCTCC-6.94
EWSR1-FLI1MA0149.1chr11:126017067-126017085CCTCCCTCCCTCCCTTCC-7.08
EWSR1-FLI1MA0149.1chr11:126017071-126017089CCTCCCTCCCTTCCTTTC-7.08
EWSR1-FLI1MA0149.1chr11:126017051-126017069CCTTCCTCCCTCCCTCCC-7.28
Foxd3MA0041.1chr11:126017775-126017787AAACAAACAAAC-6.32
NR2C2MA0504.1chr11:126017856-126017871TGACCTTTGACCTGG-7.36
Nr2f6MA0677.1chr11:126017856-126017870TGACCTTTGACCTG-7.73
RxraMA0512.2chr11:126017856-126017870TGACCTTTGACCTG-7.58
ZNF263MA0528.1chr11:126017110-126017131TCCCTCCCCTTCCTTTCCTCC-6.18
ZNF263MA0528.1chr11:126017105-126017126CTCCCTCCCTCCCCTTCCTTT-6.2
ZNF263MA0528.1chr11:126016404-126016425GCCCCTTCCCTCACCTCCTCC-6.51
ZNF263MA0528.1chr11:126017067-126017088CCTCCCTCCCTCCCTTCCTTT-6.54
ZNF263MA0528.1chr11:126017121-126017142CCTTTCCTCCCTCCCTCCCTC-6.89
ZNF263MA0528.1chr11:126017125-126017146TCCTCCCTCCCTCCCTCCCTA-6.89
ZNF263MA0528.1chr11:126016445-126016466TCCCCCACCCCCTCATCCCTC-6.94
ZNF263MA0528.1chr11:126017062-126017083CCCTCCCTCCCTCCCTCCCTT-7.05
ZNF263MA0528.1chr11:126017113-126017134CTCCCCTTCCTTTCCTCCCTC-7.11
ZNF263MA0528.1chr11:126017050-126017071CCCTTCCTCCCTCCCTCCCTC-7.19
ZNF263MA0528.1chr11:126017117-126017138CCTTCCTTTCCTCCCTCCCTC-7.48
ZNF263MA0528.1chr11:126017099-126017120CCCTCCCTCCCTCCCTCCCCT-7.54
ZNF263MA0528.1chr11:126017058-126017079CCCTCCCTCCCTCCCTCCCTC-7.97
ZNF263MA0528.1chr11:126017054-126017075TCCTCCCTCCCTCCCTCCCTC-8.08
ZNF263MA0528.1chr11:126017095-126017116TCCTCCCTCCCTCCCTCCCTC-8.08
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 4             
ChromosomeStartEnd
chr11126015889126016000
chr11126016000126016400
chr11126016400126017400
chr11126017631126017949
Number: 1             
IDChromosomeStartEnd
GH11I126145chr11126015848126018967
Enhancer Sequence
TCTCAGGAAC AAGACACACC CACTGCTTTG CTCATCCCTG TGTACCCAGT GTCTGGGATG 60
GGGTCTGGCA CCCAGAAGGC TTTCATTTGG GTGTTTGTGG AAGGCTCCTT CCCCCGTAGC 120
TGTCCTCGGC AGGGACTCAG CCTCGCGGGT CATCAGGCAG TCTCGGGGAA GTGTTCTGTG 180
CCAGGGGTCT ACTTCAGCCC CCTGTTCTGG GTGCTGCCTC GAAGGCCAGT CCCTCTGGGA 240
TGTGTGTTGG GACGGGGATT GGGTGAGCAC CCTGGGCCTT GGCAGGTGAG GTCATTCACC 300
TCTCCTTCTC TGAGGGACTT CTGGAAACTT GAGGCATCCT CTGAGCAGCG TCGTTCCTGC 360
CCTTACTTGG TCAGGAAGCT GTGATGCAGC CCAGAGACCC CCTAGTCCTT TCCTCCCCCC 420
ACTCTCCTCT CTGTGTACCT TGAGCACAAA CACTCGGAGA GCTCCTGGAG AGACGAGTTC 480
CAGCAGGAAG CAGGGGGTGT CCTGGGGGCC CAGAGAGAGA AGGCCCTGTC GTCTGTGGGG 540
GCCACAGGTC TCCACCCGTG CTCAGCCCCT TCCCTCACCT CCTCCCATCT TCCTCAGGAT 600
CCCGCTCCCC CACCCCCTCA TCCCTCTGCA CAGACCTGCC AAGTTTGGGA CATGAGAACA 660
GGCCAGGTCC CCTCTGGGGA GCCCGGGGTG GGCGGAGCCA GGCCTGGCTG GGCCTCCAGG 720
TTGGCCTGCC CTGGCCCCTG GGTTTAATAA ACTCCGAGAG AGGTTTTCAA AGGCCACTTG 780
ATCTTCCCCA TCAGGCAGCC CCTGTCTCCC TTTCAGAGCC GCGGGACTGG AAAGAAAAAA 840
CCGCTCAATG AACAAGGCGG CCAGAGAAAG CTGAGCTGCG GGGCACCTTC TATGAATTTC 900
TGATGAGCCC ACGGCCCTGA CTCCTGGGTC CCGGCCCGGT GCAGTCAGGG ATGTTAGTTT 960
AAGTCATTTC GCACGGTTCA CTGGCTCTCT GAGAGCAGCT TGTCTCCAGC CTGGGCCTCT 1020
CTAACAAGCT CTTTTTACTC AGGGCTTCTC TGAGCATAGA CCTCAAACAA TAGCAGCTTT 1080
CAAGGGGCTC GGCCCTCCTC TGGCGGCCTC CCTCTCCCAA CCCCAGCCAA GCCCAGCCTC 1140
TATCGCTCAC TGCCCACCTG AGCGCCCCCA CCCACAGCCT GACCCGCAGC GGCATTCAGG 1200
GAAGACTCGC CCCTTCCTCC CTCCCTCCCT CCCTCCCTCC CTTCCTTTCC TGTCTTCCTC 1260
CCTCCCTCCC TCCCTCCCCT TCCTTTCCTC CCTCCCTCCC TCCCTACTGC CCCTGCCCTT 1320
TCTTGCTGTA AACAGGGCAG GAGTGCGCAG TGGGGCTCTC AGGAGCAGGC CACACTGCCA 1380
CGCAACTCTA GAACACTGTG TGGATGGCAC CCCCTGGGGT TGTGCAATGA AGAGCCCCCA 1440
GTAGAACGCA GCTCATTCCA ACACTCTAAG CCTATTGGGC TCCTCAGCCC TCTTGAAACT 1500
GAGCAGTTTC CTCCTCCCTT TAGTCCAAGG AGGGAGCTGG CTTCCTCCAC ACTGCAGGCT 1560
GTCACCTGCC CCGCAGGACC CAGACCTGGT GGGGTTGATG GAGTTGCCTC CAAGAAGCGT 1620
GAAGCCGGCT CGGAGCACCT CTAGTGCCCA AGCCTGAGAG CGGACATTGG CGGCAGCGTC 1680
CCCCTGCAGA GGGGCTCCCC AGACACCAGA GGGACCGTGG CTCTCATCAG TCCAGGCCTC 1740
TCTATCTTCC CCATTCCCAC TGTTCTCCAC TGTCCCCCCT GTTCCTCAGA GCAGTGATGA 1800
GACAACTTCC AGTCCTCCCT ACCTGCCTCT GGCCTTCTTG CTCGCTAAGG GGTCTTAGGA 1860
AGAGACTCCT GGGAAGAGGT TCATTAATCA GCAGATGAGT CATTTACATG TTTAGACTAG 1920
ACCTCTGGCC AAAGCAAACA AACAAACAAA GTTCATATTG AGACAAGTCA ATATTTGACT 1980
TAATGAGAGT GCCTTGCCAG TTGAATGCTT TGATGGTGAC CTTTGACCTG GGAGCTTTGG 2040
AAGGCATTTG AGCTGCAGTC CCATGGACAC TGCACTTTGG GAGGGGCTCC AGCCCCACTC 2100
CTACAGCACC TGCCAGCAAT TAAGTTTCCC TCCCCAGGGA TCTAGGCCCT GCCTCTGGGG 2160
CCATGGGGTC TCTCACCTTT CAGGAGTCCC AGGCAGCCCA GGACTTCTTT CTTTCTGGAA 2220
GCTGCTAGAG AAAGCCCAGT TTCATGTCCC CTTTGCAAAC CCCCCCACGC TAATAACTCA 2280
CCTTCTTCAG GAAGTGAAGT CTGATCAGAG ACAGCCTGGC AAGAGGAAAG AACGAGAAAT 2340
TGGGGACAGG ACCCCGATCC CAGCTATACC TTCAACCCCT GTTTGCTGTC TGACTTTGGT 2400
GAACATTCCT GTTCTCCAGC CTGAATTCCT CATGACAGTG TGGGGACTGG ATTTCTTTCT 2460
TTCTTTTCTT TTCTTTCTTT CTTTTCTTTC TTTCTCTCCC TTTATTTCTT TTTTTTGGAC 2520
AGAGTCTCAA AGAGCAGAGT CTAAAGTGCA 2550