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

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EnhancerAtlas ID
HS088-23463 
Organism
Homo sapiens 
Tissue/cell
HeLa-S3 
Coordinate
chr17:44094640-44095980 
Target genes
Number: 2             
NameEnsembl ID
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs58879558chr1744095467hg19
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr174409563144095802
chr174409555044095600
Number: 1             
IDChromosomeStartEnd
GH17I046018chr174409567944099390
Enhancer Sequence
TCCTTATTTA TTTATTTAGA GAGGGACCCT TCTTCTGTTC CCAGGCTGGA GTGCAGTGGT 60
GCGATCTCGG CTCACTGCAA CCTCCGCCTC CTGGGTTCAA GTGATTCTCC TGCCTCAGCC 120
TCCTGAGTAG CTGAGATTAC AGGCACATGC CAACATGCCT GGCTAATTTT TTTTTTTTTT 180
TTTTTTTTTT TTTTTTGAGA TGGAGTTGTA CTCTCATTGC CCAGGCTGGA ATGTAATGGC 240
ACAATCTCGG CTCACTGCAA CCTCCACCTC CTGGATTCAA GCAATTCTCC TGTCTCAGCT 300
TCCCAAGTAG CTGGGATTAC AGGTGCCCGC CACCATGCTC AACTAATTTT TGTATTTTTT 360
TTTTAGTAGA GACGAGGTTT CACCATGTTG GTCAGACTGG TCTCAAACTC CTGACCTCAG 420
GTGATCCACC TGCCTCGGCC TCCCAAAGTG CTAGGATTAC AGGCATGAGC CACCACGCCC 480
GGCCTGAAAG GGTTCTTATT TAGTGTGCAT TTTGACATTC AATTTAATTC CAAGGTCTTG 540
TGGGGTCATG GTTTACAGGA TGTTGATATA GAAAAGACTT CACTTAATGG GCCGGGCGCA 600
GTGGCTCATG CCTGTAATCC CAGCACTTTG GGAGGCCGAG GCAGGCAGAT CAGGAGGTCA 660
GGAGATTGAG ACCATCCTGG CTAACACAGT GAAACCCCAT CTCTACTGAA AATACAAAAA 720
ATTAGCTGGG CGTGGTGGCA GGCACCTGTA GTCCCAGCCA CTCGGTTGGC TGAGGCAGGA 780
GAATGGCATG AACCCGGGAG GCGGAGCTTG CAGTGAGCAG AGACCATGCC ACTGCACTCC 840
AGCCTGGGCG ACAGAGCAAG ACTCTGTCTC AAGAAAAAAA AAAAAAAAAC AGACTTTACT 900
TACTGGAAGC CAACCAATGT ATATTTAGAG TAATTTTTCC TGGGCTGAGC TGTCATTTAC 960
TTTTGCAGTA TCTCAAGAAG AAGAGTTTAC AGTGTAAATA TTTGATGCAC ACTTTGATTA 1020
TATAGATGAA GCAAACTATT TTCAAGAGCT TTGCAAGGAC TTACTTGTAT CCAAACACCA 1080
TTCTAAAGGA GTCTTACCTA CTTCTAAAGG CTGGTCTCTA CTTGGAACCA CTTGCTTGGC 1140
CCTGGTTCAA GTCCTGCTGC AAACCTGGAA GTCCTGTCAT TGTCTTCTTC CCTCCAGAGC 1200
AGTGGCACCC AATCTAATTT TTGCTGTGCC CCAGCAGCCC CTGGCACTTT GCCCTGTAGA 1260
CTGCAGACCT CATGTAATGT ATGTTAAGTC CACAGAACCA CAGAAGATGA TGGCAAGATG 1320
CTCTTGTGTG TGTTGTGTTC 1340