EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species

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EnhancerAtlas ID
HS180-01718 
Organism
Homo sapiens 
Tissue/cell
Small_intestine 
Coordinate
chr1:53581300-53582520 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs3820201chr153581670hg19
TF binding sites/motifs
Number: 4             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
Foxo1MA0480.1chr1:53581735-53581746TGTAAACAAGA-6.02
GLIS3MA0737.1chr1:53581587-53581601CATTGTGGGGGGTG-6.01
ZNF740MA0753.2chr1:53581591-53581604GTGGGGGGTGTGG-6.03
ZNF740MA0753.2chr1:53581608-53581621GTGGGGGGTGTGG-6.03
Number of super-enhancer constituents: 4             
IDCoordinateTissue/cell
SE_33504chr1:53580602-53590875H2171
SE_50019chr1:53580320-53582842RPMI-8402
SE_63312chr1:53581598-53613108NCI-H82
SE_66967chr1:53580602-53590875H2171
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr15358172553582286
chr15358235953582445
Number: 1             
IDChromosomeStartEnd
GH01I053115chr15358126153582696
Enhancer Sequence
AGCTCTGCCA ACTGGCTGTG TGGCCTCAGG CAAGCAAGTC ACTTCCCCAT CTTTGGGCCT 60
CAGGATCTCC ATCTGTAAAA TGGGGACATC TTGGGTTTGT GCCTGGGCCC AGGCTCCTTG 120
TCACAGGGGG CTGTGTTGAG AGGGCTGTGG GTCTCTCTCC TCTCGGCTCC TCCCCACCCC 180
TAGCCACCCT GGCCTGGGCT TTCTGCCTAC CAGTGCAGGT CAGCCCCAGA GTACTGGCGT 240
CCTGGAGCCC TGGAGCCCTG GAGCCCTAGA GCAACGCTTC TTGCAGCCAT TGTGGGGGGT 300
GTGGGACGGT GGGGGGTGTG GGGTGAAGTG AGATTAATTA AGGAAATGCT TGTGCTTTGC 360
TTTGTTGACA AAAGGATTTT TCCCCAAAGC CCTTTCATTC TTTCAGATAA AGAAGTATTT 420
GTCTGGTTTT AATCATGTAA ACAAGAGCAG ATAATCCCCA GCCACGCTCC TCTTATCATT 480
AGATTCCATG CAGCAGCATC CAGCCCCAGG CTGAGCGTGA ACACCGGCCC CCTCCCCCAG 540
CGGGAGCCAC CGCCTGTGAG GGCCCTGCCC TGCCTGCTCG CTGGCGCAAT GGCTTACTCT 600
TCTGGTAAGA CACACTTTGA GCATCCCCTC TTGCAGGAAG CCGTCTCTGA CCACCAGGCT 660
GAGTGAAGCC TCCTTCTCTG GCTCCACAGT CCCTGTGCCT CCCACTGTCC CTGCCCCCAC 720
CTCACTGGAC TGCGGACTCT TTACTGGAAG CACCTCCAGG GTTGGGCCAG GTTCTGATTG 780
AATGCTGGGT CCGCAGTTTG GTAGCAGACT GCTGAGTGAA GGAGTGAGTG AATGAATGAA 840
TGAGTGTTTA CAATCTCTGC TCATCCTCAT CTGCCAGGAT GCCATATGTT AGTGATGGGC 900
TTAGGGTGGG TCTTAGACAT AAATCCTGAA GGGCTCATAA TGGGATTGTG CAGCCAGAGG 960
AAATGGGGGG CTGCCCTGCA ATCATCATCA AAGAGAGATT ATCCCACGCA GGGCCGGTGC 1020
GTCAACCCAG GGCCAAACAG TCCTCCCACC ATGACAGAAC CCCCCGCAGT GGGGTCCAGC 1080
CGCCTCAGGC CACAGGGAAG CCATGTACCC GAGAGCAGGC CCTGCCTGAG GTCACACAGG 1140
ACAGCAGTGC CCGGCTGGGC CAGAACTCAG GGCCAGACCC AGGCCTGTCC TCCTTCATTC 1200
ACGTGCATTC AAACCTTTCG 1220