Tag | Content |
---|
EnhancerAtlas ID | HS092-12347 | Organism | Homo sapiens | Tissue/cell | HFF | Coordinate | chr12:64953480-64956020 | Target genes | | | 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 |
GH12I064560 | chr12 | 64953898 | 64955793 |
| Enhancer Sequence | TTCACTCATC CTCTGGGGTC CTTATCAGGG GCCTGTGTCC CCCCCAAAAT TGTCCTCTAG 60 TCAAGGAAGT CTTGCTTTTC TAGTCTTACT TTCTAGTCTC CTTGAACAAG TACTCCCAAA 120 TCTGATTCCA AAGTTTTCCA CTGGTTCCTG CTCGCTAATT CTTATAGGTC CTTTGATATA 180 TAATCTCTTT TTTCCCTATC AGGCCCAGCC CTTCCCTGTC TTGATTATAC TGCATTTGTT 240 TATTGGCTTG GGAGACAGTA GAGGAATTGG GGGCAGCTCC TGAGAGGGCA ACCTGTTGCC 300 TTGCTGGAGA GGGATGCATT TTCATGGCCA CAACCTCCCA CCAGGTCTCC TGAAGCCAGC 360 CTTTGAAAGT GGTAGTTCTT ACTATGAAAT GATGGGCCAG CCCGGCAGAC CTGGAGGGTT 420 CAGAGGGCTC TGCCAAGTCA ACATCCTGAG AGGCATGCAT TCAGATGCCC CCATCCCATG 480 TTTCAGAGTC CCAGATTCCT CCAAACAGGG CCCTGACCTT AGCTTAACTG ACTTGCTTTA 540 GCTGAGCATT TAGGCATCTC TAGAGCTCTA GGACTATCAG AGCCTCAGTC TGTGGCTCAG 600 CTGTGGCAGT TCTTCCACTG CAGGAGAGGA GGACCCTTTT TTAAGCTACC AAACAGGTTC 660 TCTAGCTCTC ACAGTCTCTA TTGCTTGTTA TCACTTGGTG GGATGTCAAT ACAACTTAGC 720 AGTAATCAGT CAACTCTGCT CTCCCTGTAG CTATCATTCC CCCACAACCA TAGCTCTCCA 780 ATGCCTGGAT CTCTGCACCT GCACTGCATT CTCCTCCACC AGGACATCTT CCTGAATCAC 840 CACTGATGAA ATCTTTAGCA GTTGCACCAC CACATTGTGC GAGGAACTAT CCACGCCCCG 900 TATATCATTC AGGGTAGCAT CCTCTTAGCC TACTGGGCAA TGAGGGAGCC AGTCTCCAAA 960 CCCCATCTTA CTCTTGTTTT CTCAGACCAC TGCTGACATT ACTCGGGTTA GTCTGAGTTC 1020 TTTGAGAAGC AGAAGCTAAG ATGGGATTGG ATGTGCAGGA AACTCCTTAG GGAATACTTG 1080 TGCGGGATAA AGGAGAGGAG CCGAAATAGG CAAGAAGAGC CTTCAGACGC AAAGCAGGTC 1140 TGACCTCTGT GAGAGACGGG GAAGGAAGGA GGATCTGATA GGAGACTCTC AGGCTGCAGT 1200 CACAAAAGCT GCTCAGCCTG GTTGATGGGG CATCCTTGAG CCAAAGTCCG TCATTAAAAG 1260 AGTCTGTATT AGTAAAGAAT GAGTCTGTAT TAGTAAAGAA TGAGTCTGTA TTAGTACAGA 1320 ATGAGTCTGT ATTAGTTGTG CCCTGCTTGC TCAGTCATTG GCTAGCAGCA GCTTGTAGAA 1380 AGGGCGTTCT GTAAATGAGA TGGGGGTGGG TCCAGAGGTC TGCAGCTGTG GCCATTAGTC 1440 AATTATGCTC CCTGCAGCCG GAGAGCTGAG GGATGCATTT TCATGGCCAC AGCCTCCCAC 1500 CAGGTCCCTT GAAGGCTACT TATATCACTA TTGTTTGTGT ATCTTGTGAG TCATAGTATA 1560 AGGAAGCCAG ATCTAACCTC AGAGATGATT TCACGTGATG TCTTCATTTT AATGATGAAA 1620 GAAGAGAAAC TTTAAAATTT AAAATAAACT TTCCCAAGGC ACATGCATTT CAGATTGGAC 1680 CATTTTATTT TGTGTGAAGA TATTCCACGC ATTGCCGCAC ATTTGGCATT TCTGGCCCCA 1740 GGGACTAGAT GCCAGTATTC TCCCTGACCT CCTGCATCAT GACAAACAAA ATTGCTCCCC 1800 CACCACCTCA TTTCTAAAAG CTCCCTGGAG GCAATAAAGT CCCAAGTAGT ACCACTGAAC 1860 AGCTCATTGA TCTCAGAGTC AAAATGAATA TCCAAACAAG ACCCCTGTAT AATGCACTTC 1920 CATAACATCA AGAGAGCCAC TAAAACAAAA AATGCCTCAG GGAGTCACAA CCATTCCTGC 1980 TTCAGAGAGT ACTCTGCACC TCTTTAGCAT TTATCTTTTT TTTTTTTTTT TTGAGATGGA 2040 GTCTCACTAT GTCATGATCT CAGCTCACCG CAACCTCCAC CTCCTGGGTT CAAATGATTC 2100 TTGTGTCTCA GCCTCCCGAG TAGCTGGGAT TACAGGCGAG CCCAACCACG CCTGGCTAAT 2160 TTTTGTATTT GTATACAAAT ATAATGTTGG CCAGGTTGGT CTCAAAGTCT TGACCTCGAG 2220 TGATCCACCC ACCTCAGCCT CCCAAATTGC TGGGATTACG GCATGAGCCA CTGTGCATGG 2280 CCCATAGTAT TTATTTATTT ATTTATTTAT TTATTTATTT ATTTTTGTTT GTTTTGAGAC 2340 AGAGTCTTGC TCTGTTGCCC AGGCTGGAAT GCAGTGGTTG CCCAGGCTGG AATGCAGTGG 2400 TGCGATCTTG ACTCACTGCA ACCTCTGCCT CCCTGGTTCA AGAGATTCTT CTGCCTCAGC 2460 CTCCTGGGTA GCTGGGACTA CAGGCGTGCG CCACCGCACC CAGCTAATTT TAGTATTTTT 2520 GGTAGAGACA GAGTTTCGCC 2540
|
| |
|
|
|