Tag | Content |
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EnhancerAtlas ID | HS133-12138 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr17:1783990-1785550 |
Target genes | Number: 22 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
HSF1 | MA0486.2 | chr17:1784775-1784788 | TTCTGGAATGTTC | + | 6.59 | Nkx2-5(var.2) | MA0503.1 | chr17:1784461-1784472 | AAGCACTCAAG | + | 6.02 | SOX10 | MA0442.2 | chr17:1784714-1784725 | TCCTTTGTTTT | - | 6.32 | Sox3 | MA0514.1 | chr17:1784715-1784725 | CCTTTGTTTT | + | 6.02 |
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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 |
GH17I001881 | chr17 | 1784341 | 1784470 |
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Enhancer Sequence | TTTTGTGGGG CTAAACAAAG GGTTACTTGA GGCTGGGCTT TGAGAAAAGC TGGTTACAAT 60 CAGCATGGGA GCTTTCTGCC AAGCAGAAGC CTTCGTCCCT GAGTGGTGCA GCTTCCGTGT 120 TTCTTGAAGG CATTATGCCT TCTGTGAGGA GGGCTTTAAA GCCCTTAAAC GGACAAACCT 180 GTAATCCCAG GACAAACCTA GAGAGTCGGA GGAGGCAATT AGCATGTAAG TGCTGCCTGC 240 TGACCTCGAT CCTGCCAAAG GAGGGGACGG CCAGGCTTCA GCAGCGGTGT GCTGAAGGCG 300 CCTTTCTTTC CAGGGTTTAG GCTCTGGGCC TCTGTGGCGT GGGGGAACAC ATGCTTTCTT 360 TCTCTGTCAA GTCTTTGGTG CCGATCACAT CTTCTAGTGT GTATTCACTA GACTCTGATC 420 AAGTGTGGTG AGAACAATGG GCTTTTTGTT AGGATTAGAT TGTTATTCCC AAAGCACTCA 480 AGGGATGAGG AGAGCCTGTT AAAATCTCCT CACTGTATCT AGCTTTTTAG GACATTCAAA 540 CTCTGTCTTA AAAGAGTACT TCAAACTGAG ACACAGGATG CAAGAATTGA TGTGGTCAGG 600 GAAAACACTT TCACCCAAGC TTCAATAATT CCCATAGCTG TAGTCTATGG GGGGGAAGTG 660 TGTCAGTTTC CAGCTGTGTC TTAGGATTTA AGCAGCTAAA GAATGAGCTC ATTTTACATA 720 CTCCTCCTTT GTTTTGAGTC ATTTAAACCA ATGGCACTGG TGTTTGACCA GTTTCATGAA 780 GCATCTTCTG GAATGTTCAT GTCACTGAGC CATCCTCATG AGTAGTACGG TCCACACGTA 840 TCTGCCGAAC TGCAGGGCCC GTTCATAGTC TGACCAGAAC TAGCCACAGA TTTGCTTTTT 900 TCTTATTGCT TGATTTTCTT TTAGGCTCTG GAGTTCGACT CCAGGTTAAT TGCATTCCCA 960 CATTAAAATC GCATTCCCAC ATTAAAATTG CATTCCCACA TTAATGTCTT CATCTTTTAC 1020 TTGTCAATAA TCATGATCCC AGTCAACATA AAAAGCACGG CTGTCCCCAG AATAAAATAA 1080 CTTGGCATTG ATCAAAGACA AGCTCAGTGC ATACATGATA CCTGGACAAG GATTAGAGAT 1140 GTTTAGATCT TGGCTATAAC AATGCAGAGT TTTTATTGTA AGAAGGGCCG CCTTGACTCC 1200 TGACGAGTGA TCTTTGGTGG CAAATGTCTC CTTGGAGCTT TTGAAACCGT GAACTTGTGT 1260 AGCTAGTAGT GGTGAAACAG ATGGATGGGC CTTGCTGTGC CCCTGTGAGG GATTTAGCCG 1320 CTTACCTGAC AGGAGAAGGC AGCTGTCTGC AGCTCAGGGT AACATCCATT CTGTTAGATG 1380 GTCTCTGTTT AAGGAACCTG TTCTTTGTGT GGTTACCCAC CTTGGGATGG TATTTGGCCT 1440 TTCATCTCCG GCCAGCTCCT CTCCGCCACC ACTGTGTTCC CGAGCCACTT TCTCCTTGGC 1500 CCCTTTTCCT TCATATCAAT TGATGTGTGA TCAAGAAGTA CAATCAGTTT TCATAATAAT 1560
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