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

TagContent
EnhancerAtlas ID
HS095-10088 
Organism
Homo sapiens 
Tissue/cell
HMEC 
Coordinate
chr15:58684230-58685640 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs16940170chr1558684282hg19
TF binding sites/motifs
Number: 1             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
Nfe2l2MA0150.2chr15:58684526-58684541TGCTCAGTCATGTTG-6.3
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr155868424658684818
Number: 1             
IDChromosomeStartEnd
GH15I058388chr155868094158685965
Enhancer Sequence
CTTATTATAC CTTTTGACAT GGGCTGGGTG TTATTATAGA CAATACCGCC AGTGCATGGT 60
AGCCCATGGT GTTTACAGCA TGGGCTCTGG TTGAGAAACA CTGTTCTGGG TGTGTGGGAG 120
AACTCAGGGA AAGCTTCTGA TGGTGTTTCT GTCACTAAGC ATCTCACAGT CTACTATAGG 180
CTCACACTGA CTCCACCACT TATTAGTTCA TGACCTTGGG CAAGGGGCTG GACTTGTGAA 240
TATTAAATTG GCTTGTAAGG GTAAAGCAGA CAGGACAGGA CGAGGCACAC AGAATATGCT 300
CAGTCATGTT GGCTGTTTTT ATTATCGTCA TCCTTTTTAA TGAAGGTTCC TTAGCCCTAG 360
CCTACAGGTT TCTGCTGAAT TCACCACCTG AATAAGCAGC ATCAACTCAT CTGGGGGTGG 420
CAAAATGAAA GGGGAATTAG CATACGGCCC AGGGGAAAAC TTTCCCTTTG CCCTCTAAAG 480
GATTTCCTGA AAAATCCACT CACAAAAGGC AGATTTATTG AAAGGCATAT AAAATTTATT 540
TGATTACAGT TTTACAATGA CATGGGAGCC TTCCCAGTGA AGACCCAAAG ATACAGGGGA 600
AATTGTCTGT TTTTATGCTT AGGTTCAACA AAGGACGGAC AGTGTGTAGA AATACGATGG 660
GATAAAAAAG CTATGATCTA ATGCTAAAGA CTGCTTGGGG AAACCTAGCA AGGCCTGTCT 720
GGATTCTTAG CCTCTCTGAG CACGCATTCC TTCCTTCTGG GTTTGGGGCA GGGCCTTCTC 780
TGGAATTGCG GTCTTATGAC CTACAGTCAA ACAAGGTAGA TCAGATAATT TCTTTGTGGC 840
CAGTTTTTAT GCAGAAAGGT GGGGAGAGGG GAAGCGGGGA GTTAGAGTAG TATTTTTAGG 900
TCACAGGGCT GCCTTTGGGG AAAGGGGGTT CTGGTTTCTA GGACCTGCCT TGGGGAAGAA 960
GCTAGTTTCT ATATCTAGCC TTGGTGGAGA AGGAGACTAA GAGACAGGAG AGCAGAAGAT 1020
CAAAAAAAAA CTTTTGCTTC TGAGCTCTTC ATTGTGGGGT ATCACCAACA TTAGCAAGCC 1080
CCTTTCAGGA CTTTCCCAAC TCTTTTCAAT AGCCTGTTTT CACAGATCTC TCAAAACTCA 1140
AGGATTTCAA TGTCACTATT CAAGCTGAAA ACATTTTCCC CTGCAACCTC CTTGTTAAAT 1200
CTGTAGTTTG GACAAGGAAG CAATAAAGCA AGCATGTGCA GGCTGCTGCT TTGAGTAGCC 1260
AGCTGAGAAA TGATTCCCAC TAGGGTGGGT GTGGGTGTGT GTGAGTGTGT GTGTGTGTGT 1320
GTGTGTGTGC GTTGTAGGGA GAGAAAAAAT GCAATGTACA CAGCAGGATG ACCCACAGAT 1380
TCTGAGAACA CAGTGTCAGT CTGCAGAAGG 1410