EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS049-01625 
Organism
Homo sapiens 
Tissue/cell
Fetal_spinal_cord 
Coordinate
chr11:126015620-126018080 
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
AAAAATACAA AAATTAGCCA GGCATGGTGG AATACACCTG TATTTCCAGC TACTCGGTAG 60
GCTGAGGCAG GAGAATCACT TGAACCTGGT AGGCAGAGGT TGTGGTGAGC CAAGATCACG 120
CGATTGCACT CCAGCCTGGG CAACAGAGCG AGGCTCCATC TCAAAAAAAA AAAAAAAAAA 180
AAAGAACTCA CACATGTTGA TGACAGAGGG TCCCATGTCT TCTCAGGAAC AAGACACACC 240
CACTGCTTTG CTCATCCCTG TGTACCCAGT GTCTGGGATG GGGTCTGGCA CCCAGAAGGC 300
TTTCATTTGG GTGTTTGTGG AAGGCTCCTT CCCCCGTAGC TGTCCTCGGC AGGGACTCAG 360
CCTCGCGGGT CATCAGGCAG TCTCGGGGAA GTGTTCTGTG CCAGGGGTCT ACTTCAGCCC 420
CCTGTTCTGG GTGCTGCCTC GAAGGCCAGT CCCTCTGGGA TGTGTGTTGG GACGGGGATT 480
GGGTGAGCAC CCTGGGCCTT GGCAGGTGAG GTCATTCACC TCTCCTTCTC TGAGGGACTT 540
CTGGAAACTT GAGGCATCCT CTGAGCAGCG TCGTTCCTGC CCTTACTTGG TCAGGAAGCT 600
GTGATGCAGC CCAGAGACCC CCTAGTCCTT TCCTCCCCCC ACTCTCCTCT CTGTGTACCT 660
TGAGCACAAA CACTCGGAGA GCTCCTGGAG AGACGAGTTC CAGCAGGAAG CAGGGGGTGT 720
CCTGGGGGCC CAGAGAGAGA AGGCCCTGTC GTCTGTGGGG GCCACAGGTC TCCACCCGTG 780
CTCAGCCCCT TCCCTCACCT CCTCCCATCT TCCTCAGGAT CCCGCTCCCC CACCCCCTCA 840
TCCCTCTGCA CAGACCTGCC AAGTTTGGGA CATGAGAACA GGCCAGGTCC CCTCTGGGGA 900
GCCCGGGGTG GGCGGAGCCA GGCCTGGCTG GGCCTCCAGG TTGGCCTGCC CTGGCCCCTG 960
GGTTTAATAA ACTCCGAGAG AGGTTTTCAA AGGCCACTTG ATCTTCCCCA TCAGGCAGCC 1020
CCTGTCTCCC TTTCAGAGCC GCGGGACTGG AAAGAAAAAA CCGCTCAATG AACAAGGCGG 1080
CCAGAGAAAG CTGAGCTGCG GGGCACCTTC TATGAATTTC TGATGAGCCC ACGGCCCTGA 1140
CTCCTGGGTC CCGGCCCGGT GCAGTCAGGG ATGTTAGTTT AAGTCATTTC GCACGGTTCA 1200
CTGGCTCTCT GAGAGCAGCT TGTCTCCAGC CTGGGCCTCT CTAACAAGCT CTTTTTACTC 1260
AGGGCTTCTC TGAGCATAGA CCTCAAACAA TAGCAGCTTT CAAGGGGCTC GGCCCTCCTC 1320
TGGCGGCCTC CCTCTCCCAA CCCCAGCCAA GCCCAGCCTC TATCGCTCAC TGCCCACCTG 1380
AGCGCCCCCA CCCACAGCCT GACCCGCAGC GGCATTCAGG GAAGACTCGC CCCTTCCTCC 1440
CTCCCTCCCT CCCTCCCTCC CTTCCTTTCC TGTCTTCCTC CCTCCCTCCC TCCCTCCCCT 1500
TCCTTTCCTC CCTCCCTCCC TCCCTACTGC CCCTGCCCTT TCTTGCTGTA AACAGGGCAG 1560
GAGTGCGCAG TGGGGCTCTC AGGAGCAGGC CACACTGCCA CGCAACTCTA GAACACTGTG 1620
TGGATGGCAC CCCCTGGGGT TGTGCAATGA AGAGCCCCCA GTAGAACGCA GCTCATTCCA 1680
ACACTCTAAG CCTATTGGGC TCCTCAGCCC TCTTGAAACT GAGCAGTTTC CTCCTCCCTT 1740
TAGTCCAAGG AGGGAGCTGG CTTCCTCCAC ACTGCAGGCT GTCACCTGCC CCGCAGGACC 1800
CAGACCTGGT GGGGTTGATG GAGTTGCCTC CAAGAAGCGT GAAGCCGGCT CGGAGCACCT 1860
CTAGTGCCCA AGCCTGAGAG CGGACATTGG CGGCAGCGTC CCCCTGCAGA GGGGCTCCCC 1920
AGACACCAGA GGGACCGTGG CTCTCATCAG TCCAGGCCTC TCTATCTTCC CCATTCCCAC 1980
TGTTCTCCAC TGTCCCCCCT GTTCCTCAGA GCAGTGATGA GACAACTTCC AGTCCTCCCT 2040
ACCTGCCTCT GGCCTTCTTG CTCGCTAAGG GGTCTTAGGA AGAGACTCCT GGGAAGAGGT 2100
TCATTAATCA GCAGATGAGT CATTTACATG TTTAGACTAG ACCTCTGGCC AAAGCAAACA 2160
AACAAACAAA GTTCATATTG AGACAAGTCA ATATTTGACT TAATGAGAGT GCCTTGCCAG 2220
TTGAATGCTT TGATGGTGAC CTTTGACCTG GGAGCTTTGG AAGGCATTTG AGCTGCAGTC 2280
CCATGGACAC TGCACTTTGG GAGGGGCTCC AGCCCCACTC CTACAGCACC TGCCAGCAAT 2340
TAAGTTTCCC TCCCCAGGGA TCTAGGCCCT GCCTCTGGGG CCATGGGGTC TCTCACCTTT 2400
CAGGAGTCCC AGGCAGCCCA GGACTTCTTT CTTTCTGGAA GCTGCTAGAG AAAGCCCAGT 2460