| Tag | Content |
|---|
EnhancerAtlas ID | HS091-29611 | Organism | Homo sapiens | Tissue/cell | HepG2 | Coordinate | chr2:242603640-242606050 | | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| | | Number: 1 | ID | Chromosome | Start | End |
| GH02I241664 | chr2 | 242604060 | 242606201 |
| Enhancer Sequence | CAAAGTTAAA ATCCCTCCCT TGGCTAAGCA CTGTGGCTCC CGCCTGTAAT CCTAGCACTT 60
TGGGAGGTGG AGGCAGGCAG ATTGCTTGAG TCCAGGAGTT TGAGACCAGC CGCCTAGGTA 120
ACATGGTAAA ACCTCATCTC TACAAAAAAA CAAAACAAAA AAACTAGCCG GACATGGGGG 180
CATGTACCTG TAGTCCCACC TACTCGGGAG TCTGAGGTGG GAGGATCCCA TGAGCCTGGG 240
AGGTTGAGGC TGCAGTGAGA CATGATTGCA CCACTTCACT CCAGCCTGGG TGACACAGTA 300
AGACCCTGTC TCAAAAACCA AACAGAAACC CAAACAACTC CCTTAAGGCT GGGCGTGGTA 360
GCTCCTACCC ATAATCGCAC CTCTCAGGGA GGCTGAGTTG GAGGATTGCT TGAGACCAAC 420
CTGGACAACT CCCTCTCTAT AAGAAATAGA AAAATGAGGC CAGGCACATG GCTCATGTCT 480
GTAATCTCAG CACTTCGGGA GGCTGAGGTG AGCAGATCAC TTGAGGTCAG GAGTTCGAGA 540
CCAGCCCGGC CAATGTGGCA AAACCCCGTC TCTACTAAAA ATACAAAAAT TAGCTGGGCG 600
TGGTGACACA CACCTGTAAT CCCAGCTACT GGGGAGGCTG AGGCAGGAGA ATTGCTTGAG 660
CCCAGAAGGC GGAGGTTGCA GTGAACCGAG ATTATGCCAC TGCACTCCAG CCTGGACAAC 720
AGAGAATCGG CTTCAAAAAA GAAAAGTCAG GGGGCACAGT GGCCCACACC TGTTGTTCCA 780
GCTACTCGGG AGGCTGAGGC GGGAGGATTG CTTAAGTGCA GGTGTTTGAG GCTGCAGTGA 840
GCTGTGGTTG CACCACTGCA CTGCAGCCTG GGTGACAGAG TGAGACCCCG TCTCTAAAAG 900
AAATTTAAAA AGTTCTGTCT CAGAATCCTT GTTTTCCAGC TGTCTGTTTT GAGAAATTTG 960
AGTCCTACAA AAAAGTTCAG TGAGTCATGG CCACAAACCC TCCACCTAGA TCCACCAATT 1020
GTGTTTTGAC ACGCTTGGTT TTTATGAGCA AGCCTCCTAC GAATGAGAGT GTTCCTGAGA 1080
GCCACACAGC CTCATCACCA CAAAAGAGGT GACGCCACGA CTCACCAGGG TCCGTCTTGG 1140
CCCCTTGCTG TCCAGGGAAC AACCCGTGCC GCTGATTTGT GTTCCTGGTT GAGGGTCCGG 1200
TGCTGTGTGT ATATAGTTGT GATGTCTTTC TAGTCTTTAA TTGAGAAGGT TCTGCCTCTT 1260
TGTTGTGGTT GTTGCTGCTT TGTGGCATTT TTGACGAGTT CAGGTCAGCT GACCATCCCA 1320
CACGCTGGAT TTGTCTGCTT CCTCACAGTT GGGCTTGGGT TGAGCCTGTG GCTGAGAGTA 1380
GCCTCTGGGT GGCAGTGTCC TCTGCTCTCC CATCCGGGGC CTGCAGTGGG ACACTATGTC 1440
AGATCCCCGG AGATGGTGTC TTTTTTCCTT TGTAATTAAT GAATAATCCA GTGGTGACAC 1500
TGAGCATGTC CTGGTGAGCT GTGTGACTCC TGCCTGATAA TGGTGGTTTT TCTAGCCTGT 1560
CCTTTCCTTT CACGTTTATT GGTTGGCGTT CTGAGAAGAG CCGCCTTTTC TCCCATCACT 1620
TAGTGTGCAG TGTGCTACCT GTCACCTGTC TGTCACCTGT CAGTCACTGT CACCTGTCAC 1680
TGTCACTGTC ACCTGTCACT GTCCATCTTT TTGATGCTTG ACGGTTCCAC CTTTGGCCGG 1740
TGGCCACCTC AGTCTGGTGG TGTCTTTTGC CGTGTTCTGG CGTTTTTCGT TTATGTTTTG 1800
AGCCCTCCCT TATGTTCTGG GTTAAGCAGA TGCTGCAGGC ACCTCTGAAC ATTCCCTGCC 1860
TGGCCCTGGA ATCAGCCTGG CTCCTCTGAG TGGGGAGTGG TGTTGAGAAA CCTCGATCTA 1920
GACGCCGGGC ATGCTCCATG CTCCCGGAGT GTCTTCTCCC ATCACCGCAC CCTCCGGTTG 1980
ATGTGTCCTC CGGACCATTG ACTCACGGGT GTGTGTAGGC AGAAGGGGTG GAAGCGAGGA 2040
AAGGCGTTGC TGAGGAGGCC CGGAGGGAGC GGGTTCTGGC TGTGCTGGCA CTAGCCAGGC 2100
TGGCAGGCTG CGTGGGTACT TCTGTGATTT TCCTCTCAAG TGCACGTGGC TTTTTCTTGC 2160
ACTGTTTCGT GTGTGTGCTT TATTTCACAA TAAAACTCTT GAATTAAGTA TGCATAGAAA 2220
CTATTTCTTT TTTCTCTGGG TGGCAAGATT ATGAAAAAAT TTTCTTACGC TTTTCTATAT 2280
TTTCCAAGTT TGAATTTCAC TGTAAGCACC TGGCTTTGTA CCGCCCTTTT TCTGTTACAC 2340
AGTCATCATT TGCTTGCTTG TTGTGGGAGC ACTTTTGCAC AGGTCTGCTT GGTTAGTGAA 2400
AGCATGTCTC 2410
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