EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS044-02869 
Organism
Homo sapiens 
Tissue/cell
Fetal_kidney 
Coordinate
chr11:126015810-126018520 
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
CACATGTTGA TGACAGAGGG TCCCATGTCT TCTCAGGAAC AAGACACACC CACTGCTTTG 60
CTCATCCCTG TGTACCCAGT GTCTGGGATG GGGTCTGGCA CCCAGAAGGC TTTCATTTGG 120
GTGTTTGTGG AAGGCTCCTT CCCCCGTAGC TGTCCTCGGC AGGGACTCAG CCTCGCGGGT 180
CATCAGGCAG TCTCGGGGAA GTGTTCTGTG CCAGGGGTCT ACTTCAGCCC CCTGTTCTGG 240
GTGCTGCCTC GAAGGCCAGT CCCTCTGGGA TGTGTGTTGG GACGGGGATT GGGTGAGCAC 300
CCTGGGCCTT GGCAGGTGAG GTCATTCACC TCTCCTTCTC TGAGGGACTT CTGGAAACTT 360
GAGGCATCCT CTGAGCAGCG TCGTTCCTGC CCTTACTTGG TCAGGAAGCT GTGATGCAGC 420
CCAGAGACCC CCTAGTCCTT TCCTCCCCCC ACTCTCCTCT CTGTGTACCT TGAGCACAAA 480
CACTCGGAGA GCTCCTGGAG AGACGAGTTC CAGCAGGAAG CAGGGGGTGT CCTGGGGGCC 540
CAGAGAGAGA AGGCCCTGTC GTCTGTGGGG GCCACAGGTC TCCACCCGTG CTCAGCCCCT 600
TCCCTCACCT CCTCCCATCT TCCTCAGGAT CCCGCTCCCC CACCCCCTCA TCCCTCTGCA 660
CAGACCTGCC AAGTTTGGGA CATGAGAACA GGCCAGGTCC CCTCTGGGGA GCCCGGGGTG 720
GGCGGAGCCA GGCCTGGCTG GGCCTCCAGG TTGGCCTGCC CTGGCCCCTG GGTTTAATAA 780
ACTCCGAGAG AGGTTTTCAA AGGCCACTTG ATCTTCCCCA TCAGGCAGCC CCTGTCTCCC 840
TTTCAGAGCC GCGGGACTGG AAAGAAAAAA CCGCTCAATG AACAAGGCGG CCAGAGAAAG 900
CTGAGCTGCG GGGCACCTTC TATGAATTTC TGATGAGCCC ACGGCCCTGA CTCCTGGGTC 960
CCGGCCCGGT GCAGTCAGGG ATGTTAGTTT AAGTCATTTC GCACGGTTCA CTGGCTCTCT 1020
GAGAGCAGCT TGTCTCCAGC CTGGGCCTCT CTAACAAGCT CTTTTTACTC AGGGCTTCTC 1080
TGAGCATAGA CCTCAAACAA TAGCAGCTTT CAAGGGGCTC GGCCCTCCTC TGGCGGCCTC 1140
CCTCTCCCAA CCCCAGCCAA GCCCAGCCTC TATCGCTCAC TGCCCACCTG AGCGCCCCCA 1200
CCCACAGCCT GACCCGCAGC GGCATTCAGG GAAGACTCGC CCCTTCCTCC CTCCCTCCCT 1260
CCCTCCCTCC CTTCCTTTCC TGTCTTCCTC CCTCCCTCCC TCCCTCCCCT TCCTTTCCTC 1320
CCTCCCTCCC TCCCTACTGC CCCTGCCCTT TCTTGCTGTA AACAGGGCAG GAGTGCGCAG 1380
TGGGGCTCTC AGGAGCAGGC CACACTGCCA CGCAACTCTA GAACACTGTG TGGATGGCAC 1440
CCCCTGGGGT TGTGCAATGA AGAGCCCCCA GTAGAACGCA GCTCATTCCA ACACTCTAAG 1500
CCTATTGGGC TCCTCAGCCC TCTTGAAACT GAGCAGTTTC CTCCTCCCTT TAGTCCAAGG 1560
AGGGAGCTGG CTTCCTCCAC ACTGCAGGCT GTCACCTGCC CCGCAGGACC CAGACCTGGT 1620
GGGGTTGATG GAGTTGCCTC CAAGAAGCGT GAAGCCGGCT CGGAGCACCT CTAGTGCCCA 1680
AGCCTGAGAG CGGACATTGG CGGCAGCGTC CCCCTGCAGA GGGGCTCCCC AGACACCAGA 1740
GGGACCGTGG CTCTCATCAG TCCAGGCCTC TCTATCTTCC CCATTCCCAC TGTTCTCCAC 1800
TGTCCCCCCT GTTCCTCAGA GCAGTGATGA GACAACTTCC AGTCCTCCCT ACCTGCCTCT 1860
GGCCTTCTTG CTCGCTAAGG GGTCTTAGGA AGAGACTCCT GGGAAGAGGT TCATTAATCA 1920
GCAGATGAGT CATTTACATG TTTAGACTAG ACCTCTGGCC AAAGCAAACA AACAAACAAA 1980
GTTCATATTG AGACAAGTCA ATATTTGACT TAATGAGAGT GCCTTGCCAG TTGAATGCTT 2040
TGATGGTGAC CTTTGACCTG GGAGCTTTGG AAGGCATTTG AGCTGCAGTC CCATGGACAC 2100
TGCACTTTGG GAGGGGCTCC AGCCCCACTC CTACAGCACC TGCCAGCAAT TAAGTTTCCC 2160
TCCCCAGGGA TCTAGGCCCT GCCTCTGGGG CCATGGGGTC TCTCACCTTT CAGGAGTCCC 2220
AGGCAGCCCA GGACTTCTTT CTTTCTGGAA GCTGCTAGAG AAAGCCCAGT TTCATGTCCC 2280
CTTTGCAAAC CCCCCCACGC TAATAACTCA CCTTCTTCAG GAAGTGAAGT CTGATCAGAG 2340
ACAGCCTGGC AAGAGGAAAG AACGAGAAAT TGGGGACAGG ACCCCGATCC CAGCTATACC 2400
TTCAACCCCT GTTTGCTGTC TGACTTTGGT GAACATTCCT GTTCTCCAGC CTGAATTCCT 2460
CATGACAGTG TGGGGACTGG ATTTCTTTCT TTCTTTTCTT TTCTTTCTTT CTTTTCTTTC 2520
TTTCTCTCCC TTTATTTCTT TTTTTTGGAC AGAGTCTCAA AGAGCAGAGT CTAAAGTGCA 2580
GTGGCTTGAT CTCGGATCAC TGCAGGCTTG ACTCAGGCTC AGGCAATCCT CCCACCTCAG 2640
TCTCTCGAGT AGCTGGAACC ACAGGCACAC ACCACCACAC TCAGCTAATT TTGAATTTTT 2700
TGTAGAGATA 2710