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

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EnhancerAtlas ID
HS091-24095 
Organism
Homo sapiens 
Tissue/cell
HepG2 
Coordinate
chr19:40966580-40968130 
Target genes
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr194096727740967375
chr194096665340966693
Number: 1             
IDChromosomeStartEnd
GH19I040461chr194096710240968321
Enhancer Sequence
AAATAAGAGT TACCTGGTGC TGGGCGCGAT GGCTCACGCC TGTAATCCCA GCACTTTGGG 60
AGGCCAAGGC AGGTGGATCA CCTGAAGTTG GAAGTCCAAG ACCAGCCTGA CCAACACAGG 120
GAAACCCCGC CTCTACTAAA AATACAAAAT TAGCCAGGCA TGGTGGTGCA TGCCTGTAAT 180
CCCAGCTACT TGGGAGGCTG AGGCAGAAGA ATCGCTTGAA CCCAGGAGGT AGAGATTGCA 240
GTCAGCTGAG ATTGTGCCAT TGCACGCCAG CCTGGGCAAC AAGAGCGAAA CTCCGTCTCA 300
AACAAAACAA AACAAAACAA AACAAACAAC AACAACAACA ATAAACATAA AAAACCAAAA 360
AACCCAAAAA GACACAATAA AAAAATTAAA AAAAGAGATG GGGTTTTGCA TGTTGGCCAG 420
GCTGGTCTCG AACTCCTGGA CTCAAGTAAT CTGCCTGGCA TGGCCTCCCA AAGTGCTGGG 480
ATTACAGGCA TGAGCTACCG AGCGTGGCCT ATTACACCTT GTAACCATTT TGCAACTTTA 540
TCTCCTGGCC TGATCCAGGC CTACGTCTCC TTCCTGGTCC CTTTCCTGGG TCCTCCCTGG 600
GCTCCTGGAC CCAGTCCTGC CCTCTCCAAT CCATATTCCA CACAGCAGCC AGACAGAGTT 660
CTCCACAGTA ATATTTAAGT GCCTCTCTGC TCAGTTGCCT CCCGCAAGCC TGAAATGCCC 720
TGTGATAAAA CCCATGCTCC TCATGCCAGC CTTCCAGGCC CCTCGGGATC TGGCTTCTCC 780
TCTCCAGGCT CTGCTGAAGC CTCTGCCCTC TTCACCCACA GCACATTTTT TTTTTTTTTT 840
TTCTGAGACG GAGTCTCGCT CTGTTGCCCA GTCTGGAGTG CAGTGGTGCA GTCTCGGCTC 900
ACTGCAACCT CCGTCTCATG GGTTCAAGCG ATTCTCCTGC CTCAGCCTCC TGAGTAGCTG 960
TGATTACAGG CGCCTGCCAC CATGCCTGGC TAATTTTTTT GTATTTTTAG TAGAGATGGG 1020
GTTTCACGAT GTTAGCCAGG CTGGTCTCGA ACTCCTGACT GTGTGATCCA CCTGCCTCAG 1080
CCCCCCAAAG TGTTGGGATT ACAGGCATGA GCCACTGCAC CCGGCCCCAA CTGCTCTTCT 1140
TTCAGTTCCT CAAATGCATG GTGCTGCTTC CTGCCTCCTG GACTTTGCAC GTGCTGTGCC 1200
CTCTGCCTGG AACACCCTTT ACCCTCTTTA CCCGGTCCCC CCAGTAACTT GTACTTCCTC 1260
TGTCACAGCC CTCTTTATGC TGACCTGCAG CAAACCAAGC ACCCTGTGGG TCCAGGGACT 1320
GTGTCATGTT TTCTGCCATC TCCCTGAACC TTTGTAAACA CAAAAGCACA GGCATTACTG 1380
CCCCAGGGAC CTTGATCCAA ACTCCAGCTC TGCCACTTAC CAGCTGAGGA ACCTCATGCA 1440
ACCTCTTCCG TGATTGGACC TCAGCTTCCT CATCTCTGAA GTGAGGATCA CAGCACCAGC 1500
CTCCCCGTGC TATGTGACCA CCTTTCATAG GGGAATGACA CAAGATCTGT 1550