Tag | Content |
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EnhancerAtlas ID | HS101-47764 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chrX:153264610-153266070 |
Target genes | Number: 29 | Name | Ensembl ID |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH0XI154000 | chrX | 153265581 | 153265730 |
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Enhancer Sequence | CGGCCTACCC TTAATTTTTT TTTTTTGAAG TGCACAAGCT AATTTTTTAA TTACTATTTG 60 TAGAGATTAG GTCTCCCTGT GTTGCCCAGG TTGGTCTTGA ACTCCTGAGC TCACGCAATC 120 CATCTACCTT GGCCTCCCAC AATGCTGGAC TGCAGGTGTG CACCACGCTC TGGCATCATT 180 CTGGTTCTTA AACCCAAGGG TACTTATTTT CCAACATGAA CCTTAACCTC ACCCTTCCAG 240 AAACTTCTCA GGCATGGGCA AGGTTGCAGT CTCCCTTACT GCAGGCAGCA ATGACTTTAG 300 CAACAGGTGA TCTTGGTGGG CTCGTAGGGG AGTGGGAATG GGCAGTGGCT TTTGTCCTCC 360 TTTTGTTGTC CGCTGGGGAT CTTGGTTGGG AAGCCTGAAC CCAGCATTGT TTCCTAGCCC 420 TGTGTTCAAC AATGCCGGGA GCGAGGTGCC TTCCTATCCC CGTGATAAAC AGTTCTGGGA 480 CCTGTTGCTC TGCCACACAA TCCTGAGAAC TAGCACAAGT CAATTCGCTT GCAGGACCAA 540 CACACCCATG CTCCTGAAAG ATGAGACTCG CAGAGCCCGG CCCGAGACTG CACCCAGCCG 600 TCCAAGGCTG ACCATGCTTC CCACCCGGCC CTCCCCACGC CGGCTCGGAC TTCGGGCATT 660 TTCTCTCCTC CTTTCCTCCC TGGTGATCTG AGGCCGGCTC TGTCGGGGGA GTGTTCTTCC 720 TCTTTGCAGT GAGTCCAATA AACTCAGCTT TGCCTGAACA ACAGGTTTTT CTGGTGGTGA 780 TTTTGGGGAG TCTACAGCCA ACAGCTGAAA TTGGGAAAAC GGGGCGGGGG TGGGGAATCC 840 CTTTTTGTTT TTTGTTTTTA TTTTTTACAG TAAAGTGAAA GCAAGTTTAT TAGGAAGATA 900 GAGGAATAAA AGAATGGCTG CTCCATAGAC AGGGCAGCTG GGAATCCCTT TTAGCACCTG 960 GTGGCTGCAG ATGGGTAGAA ATACAGACCA TATTTGGTTC TTAGTTTAAT TAGCCAGAGA 1020 CGCAGAACAG GGTGGGAAGC CAGACGGCCA CACCTAGCAC CTCATCAGGC TGCAGCCAAC 1080 CAGGGCCTCT CGGGGCTGGG AAAACTCGAT TCTTGCTGTA CTTGGGCTTA CTCGGCTCTC 1140 CATCTTATGC AAACACCTCT CCTTATGAAA GGCAAGAAGA ATTTGTTCTA CACTGGGGAT 1200 GGGTTGTGCC TGTCACATGG AGCAGCCTGG GGACCTAGAG GGACCCTTTA GAAGCTTAGC 1260 ACCTAGCAAT TCCTTTTCAC ATGTGACTCA TGGTCTATTC AGTTTTAGTA CTTCTTTTTT 1320 TTTTGACAGA GTTTTGCTCT GTCACCCAGG CTGGAGTGCA ATGGCGCGAT CTCTGCTCAC 1380 CGCAACCTCT GCCTCCCAGG TTCAAGTGAT TCTCCTGCCT CAGCCTCCCA AGTAGCTGGG 1440 ATTACGGGCA CGCGCCACCA 1460
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