EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS034-06089 
Organism
Homo sapiens 
Tissue/cell
ECC-1 
Coordinate
chr11:126015920-126017940 
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: 2             
ChromosomeStartEnd
chr11126016000126016400
chr11126016400126017400
Number: 1             
IDChromosomeStartEnd
GH11I126145chr11126015848126018967
Enhancer Sequence
TTTCATTTGG GTGTTTGTGG AAGGCTCCTT CCCCCGTAGC TGTCCTCGGC AGGGACTCAG 60
CCTCGCGGGT CATCAGGCAG TCTCGGGGAA GTGTTCTGTG CCAGGGGTCT ACTTCAGCCC 120
CCTGTTCTGG GTGCTGCCTC GAAGGCCAGT CCCTCTGGGA TGTGTGTTGG GACGGGGATT 180
GGGTGAGCAC CCTGGGCCTT GGCAGGTGAG GTCATTCACC TCTCCTTCTC TGAGGGACTT 240
CTGGAAACTT GAGGCATCCT CTGAGCAGCG TCGTTCCTGC CCTTACTTGG TCAGGAAGCT 300
GTGATGCAGC CCAGAGACCC CCTAGTCCTT TCCTCCCCCC ACTCTCCTCT CTGTGTACCT 360
TGAGCACAAA CACTCGGAGA GCTCCTGGAG AGACGAGTTC CAGCAGGAAG CAGGGGGTGT 420
CCTGGGGGCC CAGAGAGAGA AGGCCCTGTC GTCTGTGGGG GCCACAGGTC TCCACCCGTG 480
CTCAGCCCCT TCCCTCACCT CCTCCCATCT TCCTCAGGAT CCCGCTCCCC CACCCCCTCA 540
TCCCTCTGCA CAGACCTGCC AAGTTTGGGA CATGAGAACA GGCCAGGTCC CCTCTGGGGA 600
GCCCGGGGTG GGCGGAGCCA GGCCTGGCTG GGCCTCCAGG TTGGCCTGCC CTGGCCCCTG 660
GGTTTAATAA ACTCCGAGAG AGGTTTTCAA AGGCCACTTG ATCTTCCCCA TCAGGCAGCC 720
CCTGTCTCCC TTTCAGAGCC GCGGGACTGG AAAGAAAAAA CCGCTCAATG AACAAGGCGG 780
CCAGAGAAAG CTGAGCTGCG GGGCACCTTC TATGAATTTC TGATGAGCCC ACGGCCCTGA 840
CTCCTGGGTC CCGGCCCGGT GCAGTCAGGG ATGTTAGTTT AAGTCATTTC GCACGGTTCA 900
CTGGCTCTCT GAGAGCAGCT TGTCTCCAGC CTGGGCCTCT CTAACAAGCT CTTTTTACTC 960
AGGGCTTCTC TGAGCATAGA CCTCAAACAA TAGCAGCTTT CAAGGGGCTC GGCCCTCCTC 1020
TGGCGGCCTC CCTCTCCCAA CCCCAGCCAA GCCCAGCCTC TATCGCTCAC TGCCCACCTG 1080
AGCGCCCCCA CCCACAGCCT GACCCGCAGC GGCATTCAGG GAAGACTCGC CCCTTCCTCC 1140
CTCCCTCCCT CCCTCCCTCC CTTCCTTTCC TGTCTTCCTC CCTCCCTCCC TCCCTCCCCT 1200
TCCTTTCCTC CCTCCCTCCC TCCCTACTGC CCCTGCCCTT TCTTGCTGTA AACAGGGCAG 1260
GAGTGCGCAG TGGGGCTCTC AGGAGCAGGC CACACTGCCA CGCAACTCTA GAACACTGTG 1320
TGGATGGCAC CCCCTGGGGT TGTGCAATGA AGAGCCCCCA GTAGAACGCA GCTCATTCCA 1380
ACACTCTAAG CCTATTGGGC TCCTCAGCCC TCTTGAAACT GAGCAGTTTC CTCCTCCCTT 1440
TAGTCCAAGG AGGGAGCTGG CTTCCTCCAC ACTGCAGGCT GTCACCTGCC CCGCAGGACC 1500
CAGACCTGGT GGGGTTGATG GAGTTGCCTC CAAGAAGCGT GAAGCCGGCT CGGAGCACCT 1560
CTAGTGCCCA AGCCTGAGAG CGGACATTGG CGGCAGCGTC CCCCTGCAGA GGGGCTCCCC 1620
AGACACCAGA GGGACCGTGG CTCTCATCAG TCCAGGCCTC TCTATCTTCC CCATTCCCAC 1680
TGTTCTCCAC TGTCCCCCCT GTTCCTCAGA GCAGTGATGA GACAACTTCC AGTCCTCCCT 1740
ACCTGCCTCT GGCCTTCTTG CTCGCTAAGG GGTCTTAGGA AGAGACTCCT GGGAAGAGGT 1800
TCATTAATCA GCAGATGAGT CATTTACATG TTTAGACTAG ACCTCTGGCC AAAGCAAACA 1860
AACAAACAAA GTTCATATTG AGACAAGTCA ATATTTGACT TAATGAGAGT GCCTTGCCAG 1920
TTGAATGCTT TGATGGTGAC CTTTGACCTG GGAGCTTTGG AAGGCATTTG AGCTGCAGTC 1980
CCATGGACAC TGCACTTTGG GAGGGGCTCC AGCCCCACTC 2020