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

TagContent
EnhancerAtlas ID
HS092-37541 
Organism
Homo sapiens 
Tissue/cell
HFF 
Coordinate
chr8:131525860-131527300 
Target genes
Number: 1             
NameEnsembl ID
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr8131526366131527296
Number: 1             
IDChromosomeStartEnd
GH08I130513chr8131525845131527565
Enhancer Sequence
GTTAGGTCCA TAAGAGTAGG GTCGGAACTG TCCTGTTTGT TGCCAAATCG CCATTGCCTA 60
GAACAGGGCC TTACACCCTA ACTGGTGCTC AATAAATGTT CCTCGAGTGC ATGATAAAGA 120
GATGTACAGG TAAATAGCAT TCTCTCAGGG TCCAGAGTAG AAGAGATTAC TCTGACTGAC 180
TGGTTGGAGA AGGTTGGATT CAGGACCAGC TTCGTGATTT TTGGGGCCCA GTAAAAATTG 240
AAAATTCAAC ACTGCTATTT CAAAAATGGT TACAAATTTC AATTTGGTGA CAGCAGAGCA 300
TTAAAGCATT AATTTGGAGT CCTTCCAAGT ATGGAGGCCT GTGTGACTGC ACAGGTCACA 360
GGCCCCTGAA GCCACCCTGG CTGGAGTTGA TTCTGGAAGG CGTCATAGGG GAGGAGGCAT 420
TGGAGCTGCT TCAAATCTGG GACTGGGAAA GGACATTCTC AGAGAAAGGA ATAGAATAGC 480
ACAGGCAGGG GGTGGACAAC TGCCCAGGGA GCATTGAGTC CTGATTAAAG GCCAGGGGAA 540
GTGGGTGGAT ATTTTCTTGT ACTGTTTAAA AAAAATAAAA AAGGCAAGTC TCCCTCCTCT 600
GAGCTCTATT TTGGGGTGGG TTTTATTAAT AACAGATGAG CCTGGGCTCT GGGGACCTCA 660
GGAGTAATTC ATCATTTTCA TCAGGGCTTG ATGAGGCCTC AGAACCATGC AGAAGCTCAT 720
CCTGAATCAT TTCGGGGTTT TTTTTTTTTT TTCCTTTTTC TGCTTAGCAA TTGAACAGGC 780
GCCACCAGCA AGGAGGGCCT TTGCTCAAAC ACAAACCCTT GGCACGATGC CCGCCGATGT 840
CAGCAACTGT GCTGCCTGGC ATCTGCTGTG GTGAGGTCAG AATGGAGCAT GCTGCCTTGT 900
GTTTGCATGC CAGCAAGGGG GTGACAGACG CGATATTGGG TGGAAGAAAA CATGCGCGGG 960
CTATGCTGGT GGCAGAGTGA GGTCTGGGGG CTGGTATGAG AGGGAGACCG GTCAAAGAGG 1020
TGGCTTGTCA GGTTAAAGAG CGTGAGTACC ACTGTAGGAG CTCTGCGAGG CTTGGCTGGT 1080
AAGAGTGACT TTGCACTTCG TGCTACTCTC CTAGGGCAGC TGTAACCAGC AACCACAAAC 1140
TGGGTATCTT AAAAGGACAG AAATGGATTC TCTCACAGTT CTGGAGGCCA GAAATTCCCA 1200
GTCAAGGTGT TGGCAGGGCC ATGCTCCCTC TGAAGGCTCT AGGGGACCTT CCTTGCCCCT 1260
TCAAGCTTCT GGTGGCTCCT GGCAATTCTT GGCATTACTC AGCTTACAGC TGCATTATTC 1320
CAGTTTCCGC CTTTGTTGTC ATATGGTGCA CTTCCCTCTG TGTTTTTTCC AAGCTCCCCT 1380
TTCTTGTGAG AACACTGGCT GGGCTCTGTG GCTCATGCCT GTAATCCCAG AACTTTGGGA 1440