Tag | Content |
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EnhancerAtlas ID | HS113-01190 |
Organism | Homo sapiens |
Tissue/cell | Keratinocyte |
Coordinate | chr1:53384110-53385780 |
Target genes | Number: 13 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
SOX10 | MA0442.2 | chr1:53384222-53384233 | GTCTTTGTTTT | - | 6.14 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr1 | 53385177 | 53385318 | chr1 | 53385495 | 53385549 |
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Enhancer Sequence | TTATCATAGG AGATGGCAGC TCCATGCACG TTATCGCCCC TGAAGACCTT CCAGTGGGAC 60 AAGATGTGGA GGTGGAAGAC AGTGATAGGT CTAGGCTCGT GTGTGTGCTT GTGTCTTTGT 120 TTTTAACAAA AAAAGTTTAA GAATTAAAAT TTTTAAAAGC TTATAAAATA AGGATCTAAA 180 GAAGAAAACA TTTTTTGTAC AGCCGTACAA TGTGTTTGTG TTTTAAGCTG AGTGTTACTA 240 CAAAAGAGTC AAAAGTTGAA AAAATTAAAA AGTTTATAAA GTAAAAACAG AGTAAGCTAA 300 GGTTAATTTA TCATTGAAGA AAGAAACATT TGTAAAGCAA ATTTAGTGTA GCCTAGGTGT 360 ACAGTGTTAT AGAGTCTATA GTAGTGTACA GTAATGTCCT AGGCCAGGGG TCCCCAACCC 420 CCGGGCTGTG GACCCATCCC AGTCTGTGGC CTGCTAGGAA CTGGGCCACA CAACAGGAGA 480 TGAGCAGCTT CATCTGTATT TACAGCAGCT CCCCATGGCT TGAATTACCA CCTGAGTTCC 540 ACCTCCTATC AGATCAGTGG TGGCATTAGA ATCTCATAGG AGTGCGAACC CTATTGTGAA 600 CTGTGCATGT GAGGAATCTA GGTTGTTGCG AGCTCCTTAT GAGAATCTAA TGCCTGATGA 660 TCTGAGGTGG AACAGTTTCA TCCCCAAACC ATCTGTCCGC CCGCAAGTCC ATGGAAAAAC 720 TGTCTTTCAT GAAAATAGTC CCTGGTGCCA AACCAGTCCC TGCTGTCCTA GGCCTTCACA 780 TTCACTCACC ATTCACTCGC TGACTCACCC AGTGCAGCTT CCAGTCCTGC AAGCTCCATT 840 TATGGTAACT GCCCAGTACA GGTGTACTAT TTAAAAAATC TTTTAGACTG TATTTTTACT 900 GTGCCTTTTC TATGTTCAGA TACACATTTA CCATTGTGTT ACAGTTGCCT ACAGTATTCA 960 GCCCGGTACC ATGCTGTCCA GGTTTGTATT CTAGGAGCAA CAGGCTATAC ACCATGTAGC 1020 CTTGGTGTGC AGTAGGCTAC CCCATCTAGG ACTGTGTAGG TGCACTCTGT GATGCTCCCA 1080 CAATGACCAC AATCACCTAA TGATGCATTT CTCAGAATGT AGCCCCGTTG TTAAGCAACA 1140 CATGACTCTA TGAGAAATAA AGCCGCTAAG AACAGTGAAG AATGGTTTAC CACCCAACCT 1200 CAAGCTCAAA GGCAGCAGGT AAAATGTAAC AGTGCTCTTG TGCCATCAGC CCCAGTGGAA 1260 GGCAGAACCT GCAGCTTCTA ATATGAACAT CAAATGACCC CAACTCATTC CCTGTGAGGG 1320 CTCCGTGTGT GATCTCATCC CCATGCCTCC TCTGCACTGT CATCTTGGTT TCTGTCTCTC 1380 CTTCTCTCAC TGCCTTTTCC TGCCCTTTGA GCCCTCTGGC AGGGGCAGAG GCTTAATCTG 1440 CTGATCCTTG TCATTCTTTT TTGGATAAAA TGATTCCCGA TATTTGCAAG TGAGCCTAAA 1500 GGTCTTTAAC CCATGATAAT TTTGTGTTTA CACATGTACA AGTCTGTATT TTGAGTCACT 1560 GAATTACTAG AAGAGCCAGT GATTACCTAA TGGTTGAGAA CACAGGCTTT GAAATCAGAC 1620 CTGGTTCAAA TAACTTAACC TTCTGTGCCT CAGTTTTTTA ATCTGTAAAG 1670
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