EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS045-13680 
Organism
Homo sapiens 
Tissue/cell
Fetal_lung 
Coordinate
chr11:126016230-126018160 
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
chr11126016400126017400
chr11126017631126017949
Number: 1             
IDChromosomeStartEnd
GH11I126145chr11126015848126018967
Enhancer Sequence
CCAGAGACCC CCTAGTCCTT TCCTCCCCCC ACTCTCCTCT CTGTGTACCT TGAGCACAAA 60
CACTCGGAGA GCTCCTGGAG AGACGAGTTC CAGCAGGAAG CAGGGGGTGT CCTGGGGGCC 120
CAGAGAGAGA AGGCCCTGTC GTCTGTGGGG GCCACAGGTC TCCACCCGTG CTCAGCCCCT 180
TCCCTCACCT CCTCCCATCT TCCTCAGGAT CCCGCTCCCC CACCCCCTCA TCCCTCTGCA 240
CAGACCTGCC AAGTTTGGGA CATGAGAACA GGCCAGGTCC CCTCTGGGGA GCCCGGGGTG 300
GGCGGAGCCA GGCCTGGCTG GGCCTCCAGG TTGGCCTGCC CTGGCCCCTG GGTTTAATAA 360
ACTCCGAGAG AGGTTTTCAA AGGCCACTTG ATCTTCCCCA TCAGGCAGCC CCTGTCTCCC 420
TTTCAGAGCC GCGGGACTGG AAAGAAAAAA CCGCTCAATG AACAAGGCGG CCAGAGAAAG 480
CTGAGCTGCG GGGCACCTTC TATGAATTTC TGATGAGCCC ACGGCCCTGA CTCCTGGGTC 540
CCGGCCCGGT GCAGTCAGGG ATGTTAGTTT AAGTCATTTC GCACGGTTCA CTGGCTCTCT 600
GAGAGCAGCT TGTCTCCAGC CTGGGCCTCT CTAACAAGCT CTTTTTACTC AGGGCTTCTC 660
TGAGCATAGA CCTCAAACAA TAGCAGCTTT CAAGGGGCTC GGCCCTCCTC TGGCGGCCTC 720
CCTCTCCCAA CCCCAGCCAA GCCCAGCCTC TATCGCTCAC TGCCCACCTG AGCGCCCCCA 780
CCCACAGCCT GACCCGCAGC GGCATTCAGG GAAGACTCGC CCCTTCCTCC CTCCCTCCCT 840
CCCTCCCTCC CTTCCTTTCC TGTCTTCCTC CCTCCCTCCC TCCCTCCCCT TCCTTTCCTC 900
CCTCCCTCCC TCCCTACTGC CCCTGCCCTT TCTTGCTGTA AACAGGGCAG GAGTGCGCAG 960
TGGGGCTCTC AGGAGCAGGC CACACTGCCA CGCAACTCTA GAACACTGTG TGGATGGCAC 1020
CCCCTGGGGT TGTGCAATGA AGAGCCCCCA GTAGAACGCA GCTCATTCCA ACACTCTAAG 1080
CCTATTGGGC TCCTCAGCCC TCTTGAAACT GAGCAGTTTC CTCCTCCCTT TAGTCCAAGG 1140
AGGGAGCTGG CTTCCTCCAC ACTGCAGGCT GTCACCTGCC CCGCAGGACC CAGACCTGGT 1200
GGGGTTGATG GAGTTGCCTC CAAGAAGCGT GAAGCCGGCT CGGAGCACCT CTAGTGCCCA 1260
AGCCTGAGAG CGGACATTGG CGGCAGCGTC CCCCTGCAGA GGGGCTCCCC AGACACCAGA 1320
GGGACCGTGG CTCTCATCAG TCCAGGCCTC TCTATCTTCC CCATTCCCAC TGTTCTCCAC 1380
TGTCCCCCCT GTTCCTCAGA GCAGTGATGA GACAACTTCC AGTCCTCCCT ACCTGCCTCT 1440
GGCCTTCTTG CTCGCTAAGG GGTCTTAGGA AGAGACTCCT GGGAAGAGGT TCATTAATCA 1500
GCAGATGAGT CATTTACATG TTTAGACTAG ACCTCTGGCC AAAGCAAACA AACAAACAAA 1560
GTTCATATTG AGACAAGTCA ATATTTGACT TAATGAGAGT GCCTTGCCAG TTGAATGCTT 1620
TGATGGTGAC CTTTGACCTG GGAGCTTTGG AAGGCATTTG AGCTGCAGTC CCATGGACAC 1680
TGCACTTTGG GAGGGGCTCC AGCCCCACTC CTACAGCACC TGCCAGCAAT TAAGTTTCCC 1740
TCCCCAGGGA TCTAGGCCCT GCCTCTGGGG CCATGGGGTC TCTCACCTTT CAGGAGTCCC 1800
AGGCAGCCCA GGACTTCTTT CTTTCTGGAA GCTGCTAGAG AAAGCCCAGT TTCATGTCCC 1860
CTTTGCAAAC CCCCCCACGC TAATAACTCA CCTTCTTCAG GAAGTGAAGT CTGATCAGAG 1920
ACAGCCTGGC 1930