| Tag | Content |
|---|
EnhancerAtlas ID | HS091-36106 | Organism | Homo sapiens | Tissue/cell | HepG2 | Coordinate | chr4:938020-940880 | SNPs | | Number: 2 | ID | Chromosome | Position | Genome Version |
| | | 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 |
| GH04I000945 | chr4 | 938989 | 939388 |
| Enhancer Sequence | CAGTGAGCTG CGATCGTGCC ACTGCAATCC AGCCTGGGCG ACAGAGCAAG ACTGTCTCAA 60
AAAAATAATT AACTAAATAA ACGAGGCAAA ATTACAGTGA CAGAAAACAG ATCAGTGGTT 120
GCTGGAGCTT GGGGTTGGGG AAGCTTGAAC ACAAAGATGC TGTTTGGGGA TAGAACAGTT 180
TGCTGGATTG TGGCTAGCTG TGGTTACATG CCTGTCTGCA TTCTAGGTAA GAAGTAACCT 240
GGGCATAGAG CAAAAGCCCC CCACCTGCTC CCCGCCCCTC CCTGCCTGGG TTGCTGCAGC 300
GCTGTCTGGA AGTTGGCGAA CATTGTTCTT ATTTGTGGTT TTCATTTCTT ACCGTATACA 360
CATACGGTGT GTGTATAATT AAGAAGATAG ATGGTTTTAT GTGTCCATTG TTTACATAAA 420
TGGTACAATA GTATGGTTTT GCAACTTGAT TTTTTTGTCT CAACATTTTG TTTTATAGTT 480
CTATACTTGT AGATCTGTTT TAACTTTCTG ATAGTTTACT TCATGGTTTA ATGATTTGTC 540
CCTTACTAGT CAGAATGTGT TTTAGTTTTA TTGTTAAAAC ACACCGGGCT GGCTGCGGTG 600
GCTCTCGCCT GTAATCCAAG CACTTTGGGA GGCTGAGGCA AGGAGATTGC TTGAGCCCAG 660
GACTTCAAGA CCAGCCTGGG CAACATGATG AAACCCCTGT CTCTATGAAA AATACAAAAA 720
ATTAGCCAGG CTTGGTGGTG CACGCCTGTA GTCCCAGCAA CACAGGAGGC TGAGGTGGGA 780
GGATCACTTG AGCCTAGGAG GTCGAGGCTG CAGTGAGCCG TGATTACGCC ACTGCCCTCC 840
AGCGTGGGCA ACAGACTGAG ACCCTGTCTC AAAAAGAAAA AAAGAAAAAC TGCGTGTTGC 900
CTCAGTGCAG ACCCTAGGCA GCCTGTCATG GCAGTCCCAG TGAGACTGCC TGGAATGGAC 960
CCTTGGAGGG TATGGCACTA CACCTTATTA ACTGTTGCTA AACTGTCGCT GAAACACACA 1020
TGTCCGTTTA CATTCCTGCC TCAGTTTCTG TTTCCCCAGG CCCCCGCCGT CTCTGTCTCC 1080
TCACTCCCCG CCGTTTGTTG CTGCCTCAGC TTCTGTTTTC CCCACGTCTT TGCCGTCCTG 1140
TCGTCTCACT CCCCGCCGTC TGTCCCCACC GTTCATTCCA GCCTCGGTTT CTGTTTTCCC 1200
CAGGTCCCTG CCCTCCCGTC GCCTCACGCC CACCACCCTG GCTGGCCTCT CTCCGTTTCA 1260
TTTGCACCTC CCCGATCTCC CTGATTGCTA GTGAAGTGGA ATGCCTTGTG TGTTTGTTTT 1320
TCCCGGCTGG AAACCAGTGA GCCTCTGTCC ATTCTCTGGG GTGAACTCTC CTTGTTTTTG 1380
TGCGTCTCGC CTTGGTGTGA GCAGACTACA GCACATCCCT CTTCCTGCGG ACCCTCTAGC 1440
TGGCCACATA TTTCAGTCCC CTGATGCCCT TGGCCAAGTA AACAGCACCC CCTTTGGAGT 1500
AAAACCTGGG GGCTCTGGCT TGTCACCTCC CGCTGGTGCT GAAGGGCTCT CCCCATACCC 1560
TTCCTGAAGA GGTCTCCGCC CCTTAAATGG TGGAGAGCCC AGCCTGTCCT GCCCCCGGCT 1620
GCTCCTCTCC TCCTTCCCGG GTGCCACTCC CTCGGACCAC CCCCACATTT CCAAGTAGCA 1680
CAGAAATTAC TTCTGTTTCT AACACGGCTC AATCCGAGGT ACCTTTGAAG GCTGCAGCTC 1740
CAGCCTGACT CCTTCCATCC CCATAGCTCC CCTGCCCTGA GACAGCCTCC GGTGCTTCTG 1800
CTGTGTCCCA GGAAACAAGC CTGAAGCAAG CACTCACCAT CCCTCAAGAA TGTGCCCTGA 1860
CCTACCTTCC TCACCACGGT GGCATCAGGG CCAGGTGGGC TCCCCCTTCT CCGTCACCCC 1920
CCACGGCAGC CCCCAATACT CTTAGGAGCT GCTTTCCCAC ATGCTGTGTG TCTCCTGGGA 1980
TGCCAGACCT CCGTCACTCC TCTCCTAGGT CATAGCAGCC CTTCTGACTG GCGTCCTTGA 2040
CACACTGCTG CCCTCTTCCC TGCTCCGGGG CACCTGGCTG CAGGTGGGGC TCAGCCAACA 2100
TGGGGCTCTC TGGCCACATT CTATGTTTGG GGAACTTGTC TCAGTGTGCC CAGCCTCCAC 2160
CTCGGGTGCA GGGTGAAATC CATAGTGCCT GGTTGGCACG AGGCTGCCCA CTCGGGTGCA 2220
GGGTGAAATC CATAGTGCCT GGTTGGCACG AGGCTGCCCA CTCGGGTGCA GGGTGAAATC 2280
CATAGTGCCT GGTTGGCACG AGGCTGCCCA GCACCATGCA GCAATGGCTC CTGCAGCCAT 2340
ACCTCAGTTC TGTCTCCGTG AGGCGCTGGG GTCTCTTCTG TCCAGAGTAC TCTCCACCTG 2400
GCATCTTATT CATCTTCCCA GATGCATCTC TGATATTAAA AATGCCTGGG GAGTGCTGTG 2460
CTGAGCCACA GCTGTGGCGT GTGCCCAGTG TGCACCCAGC CCCGGCTCCC ACAGGCGGAC 2520
TGGAGTGCCT GCCCTGGTGC TAACTGGCTA CATATGCAGG GCCTTGGTTT CCCCAAAGGT 2580
CACCAAGGGA GAGCGCGGCC CCTGTAGGAA ACAGCCCCAG GCACGCGTGC ACAGGCGCCG 2640
AGACCGAGGG AGAGCGCGGC CCCGTAGGAG ACAGCCCCAG GCACGCGTGC ACAGGCGCCG 2700
AGACCGAGGG AGAGCACGGC CCCTGTAGGA GACAGCCCCA GGCACGCGTG CACAGGCGCC 2760
GAGACCGAGG GAGAGCGCGG CCCCTGTAGG AGACAGCCCC AGGCACGCGT GCACGGGCGC 2820
CGAGACCGAG GGAGAGCGCG GCCCCTGTAG AGAACAGACA 2860
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