EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS175-05323 
Organism
Homo sapiens 
Tissue/cell
SK-N-MC 
Coordinate
chr11:126015820-126018530 
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: 5             
ChromosomeStartEnd
chr11126015889126016000
chr11126016000126016400
chr11126016400126017400
chr11126015834126017988
chr11126017631126017949
Number: 1             
IDChromosomeStartEnd
GH11I126145chr11126015848126018967
Enhancer Sequence
TGACAGAGGG TCCCATGTCT TCTCAGGAAC AAGACACACC CACTGCTTTG CTCATCCCTG 60
TGTACCCAGT GTCTGGGATG GGGTCTGGCA CCCAGAAGGC TTTCATTTGG GTGTTTGTGG 120
AAGGCTCCTT CCCCCGTAGC TGTCCTCGGC AGGGACTCAG CCTCGCGGGT CATCAGGCAG 180
TCTCGGGGAA GTGTTCTGTG CCAGGGGTCT ACTTCAGCCC CCTGTTCTGG GTGCTGCCTC 240
GAAGGCCAGT CCCTCTGGGA TGTGTGTTGG GACGGGGATT GGGTGAGCAC CCTGGGCCTT 300
GGCAGGTGAG GTCATTCACC TCTCCTTCTC TGAGGGACTT CTGGAAACTT GAGGCATCCT 360
CTGAGCAGCG TCGTTCCTGC CCTTACTTGG TCAGGAAGCT GTGATGCAGC CCAGAGACCC 420
CCTAGTCCTT TCCTCCCCCC ACTCTCCTCT CTGTGTACCT TGAGCACAAA CACTCGGAGA 480
GCTCCTGGAG AGACGAGTTC CAGCAGGAAG CAGGGGGTGT CCTGGGGGCC CAGAGAGAGA 540
AGGCCCTGTC GTCTGTGGGG GCCACAGGTC TCCACCCGTG CTCAGCCCCT TCCCTCACCT 600
CCTCCCATCT TCCTCAGGAT CCCGCTCCCC CACCCCCTCA TCCCTCTGCA CAGACCTGCC 660
AAGTTTGGGA CATGAGAACA GGCCAGGTCC CCTCTGGGGA GCCCGGGGTG GGCGGAGCCA 720
GGCCTGGCTG GGCCTCCAGG TTGGCCTGCC CTGGCCCCTG GGTTTAATAA ACTCCGAGAG 780
AGGTTTTCAA AGGCCACTTG ATCTTCCCCA TCAGGCAGCC CCTGTCTCCC TTTCAGAGCC 840
GCGGGACTGG AAAGAAAAAA CCGCTCAATG AACAAGGCGG CCAGAGAAAG CTGAGCTGCG 900
GGGCACCTTC TATGAATTTC TGATGAGCCC ACGGCCCTGA CTCCTGGGTC CCGGCCCGGT 960
GCAGTCAGGG ATGTTAGTTT AAGTCATTTC GCACGGTTCA CTGGCTCTCT GAGAGCAGCT 1020
TGTCTCCAGC CTGGGCCTCT CTAACAAGCT CTTTTTACTC AGGGCTTCTC TGAGCATAGA 1080
CCTCAAACAA TAGCAGCTTT CAAGGGGCTC GGCCCTCCTC TGGCGGCCTC CCTCTCCCAA 1140
CCCCAGCCAA GCCCAGCCTC TATCGCTCAC TGCCCACCTG AGCGCCCCCA CCCACAGCCT 1200
GACCCGCAGC GGCATTCAGG GAAGACTCGC CCCTTCCTCC CTCCCTCCCT CCCTCCCTCC 1260
CTTCCTTTCC TGTCTTCCTC CCTCCCTCCC TCCCTCCCCT TCCTTTCCTC CCTCCCTCCC 1320
TCCCTACTGC CCCTGCCCTT TCTTGCTGTA AACAGGGCAG GAGTGCGCAG TGGGGCTCTC 1380
AGGAGCAGGC CACACTGCCA CGCAACTCTA GAACACTGTG TGGATGGCAC CCCCTGGGGT 1440
TGTGCAATGA AGAGCCCCCA GTAGAACGCA GCTCATTCCA ACACTCTAAG CCTATTGGGC 1500
TCCTCAGCCC TCTTGAAACT GAGCAGTTTC CTCCTCCCTT TAGTCCAAGG AGGGAGCTGG 1560
CTTCCTCCAC ACTGCAGGCT GTCACCTGCC CCGCAGGACC CAGACCTGGT GGGGTTGATG 1620
GAGTTGCCTC CAAGAAGCGT GAAGCCGGCT CGGAGCACCT CTAGTGCCCA AGCCTGAGAG 1680
CGGACATTGG CGGCAGCGTC CCCCTGCAGA GGGGCTCCCC AGACACCAGA GGGACCGTGG 1740
CTCTCATCAG TCCAGGCCTC TCTATCTTCC CCATTCCCAC TGTTCTCCAC TGTCCCCCCT 1800
GTTCCTCAGA GCAGTGATGA GACAACTTCC AGTCCTCCCT ACCTGCCTCT GGCCTTCTTG 1860
CTCGCTAAGG GGTCTTAGGA AGAGACTCCT GGGAAGAGGT TCATTAATCA GCAGATGAGT 1920
CATTTACATG TTTAGACTAG ACCTCTGGCC AAAGCAAACA AACAAACAAA GTTCATATTG 1980
AGACAAGTCA ATATTTGACT TAATGAGAGT GCCTTGCCAG TTGAATGCTT TGATGGTGAC 2040
CTTTGACCTG GGAGCTTTGG AAGGCATTTG AGCTGCAGTC CCATGGACAC TGCACTTTGG 2100
GAGGGGCTCC AGCCCCACTC CTACAGCACC TGCCAGCAAT TAAGTTTCCC TCCCCAGGGA 2160
TCTAGGCCCT GCCTCTGGGG CCATGGGGTC TCTCACCTTT CAGGAGTCCC AGGCAGCCCA 2220
GGACTTCTTT CTTTCTGGAA GCTGCTAGAG AAAGCCCAGT TTCATGTCCC CTTTGCAAAC 2280
CCCCCCACGC TAATAACTCA CCTTCTTCAG GAAGTGAAGT CTGATCAGAG ACAGCCTGGC 2340
AAGAGGAAAG AACGAGAAAT TGGGGACAGG ACCCCGATCC CAGCTATACC TTCAACCCCT 2400
GTTTGCTGTC TGACTTTGGT GAACATTCCT GTTCTCCAGC CTGAATTCCT CATGACAGTG 2460
TGGGGACTGG ATTTCTTTCT TTCTTTTCTT TTCTTTCTTT CTTTTCTTTC TTTCTCTCCC 2520
TTTATTTCTT TTTTTTGGAC AGAGTCTCAA AGAGCAGAGT CTAAAGTGCA GTGGCTTGAT 2580
CTCGGATCAC TGCAGGCTTG ACTCAGGCTC AGGCAATCCT CCCACCTCAG TCTCTCGAGT 2640
AGCTGGAACC ACAGGCACAC ACCACCACAC TCAGCTAATT TTGAATTTTT TGTAGAGATA 2700
GGGTTTTGCC 2710