Tag | Content |
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EnhancerAtlas ID | HS133-26070 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr6:683140-684400 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NHLH1 | MA0048.2 | chr6:683931-683941 | CGCAGCTGCG | + | 6.02 | NHLH1 | MA0048.2 | chr6:683931-683941 | CGCAGCTGCG | - | 6.02 | ZNF263 | MA0528.1 | chr6:684166-684187 | GAAGGATGAGGTTAGGGAGGG | + | 6.17 | ZNF263 | MA0528.1 | chr6:684208-684229 | GGGGGAGGGGAGACAGGAGAG | + | 6.8 |
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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 |
GH06I000679 | chr6 | 679921 | 685725 |
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Enhancer Sequence | CTGACCTTGC GGGAAGATGT GAGTGGCCTA GACTTTCTAA TCCTTGACAA ACATCAACAC 60 CACCAACTCC ATTCCAGCAA GACTGCCAGG AAGACATGAA AATAAAGAAG CTAAACAATG 120 CAAAATCCCA AGTGATATCA AGAGTCTACA TATGTTTATT CAAATAACAA AATACTTGAC 180 CATCTCAACA ATAATGTTCA GGAATGAGAG AGGAACAAAA TCAAGAAAAT ATTACTAAGC 240 TATTCATAAT GAAAGGATTG GATAAAAAGA TATTCTCCTA AATTTATACT ACTACATAAA 300 AACAAAGTTT CATTTGTCTC GACTTGTCAA ATCTTTAGGA TGAAATAAAC CAATATCACC 360 GCTGACAAAT ATAATAACTA TGGTAAACAG GCATGCCAAA ATCAATGCAG AGTTTCAGAA 420 AAGGTCAAGA AACCAACCGT CAGCTTAAAT TGGTTAATTT CATTAAAACT GTTAAACATG 480 ACAGGATGTC GCTAACTCCC AGGTTCTTTT ATATGAGCAA AGTTGGATTA ATTTGACCCA 540 AATTTTGTAT AATAGCTTTT CCAATTTCCA AAAATACATC AACTTTGTCA CTGATCTTAC 600 AAATTCTGCT TTCCTTCTCT AGCTCTATCT CAAAAGAAGC TTCTCGAAGG CCATAAATCT 660 TGACATAGTG AAAGCAAAAT AATCACAGCA CTCAACAGTG CCGTTAACAT TTCTGAGCCG 720 TGAGGGATTA AGCAGGCAGA TGCTATGGAA AGTGCCTGTC AGGAAAGGAC AGCCCAGAGT 780 TCAGAACGCA CCGCAGCTGC GAAGGATTGA AGCTGCTAGC TATGGAATCA AGCTCAGGAG 840 AAACTCTGGG CACAATTCCG GCATCCGAAA TAAATTAAAG TAAACAGTGT TGCTCTCTCT 900 CTCATCCACC CTGTTAGCAG CCTCTCGGCT GAGCGGGAGA CCACACACTC GGACCACACA 960 GCGCCAGCTG AACTCCCTCG CACGCAACAT CTACAAGCTG TCACTCTGCA GCAGCCCAGA 1020 GAGGGAGAAG GATGAGGTTA GGGAGGGGGA GACAGGACCG CAGGAAGAGG GGGAGGGGAG 1080 ACAGGAGAGT CTTCCCTATG TGCAGCTGGA GAGAGTGATG TGTGGTTTAG AGAAGGGGGA 1140 GGGGTGGAAT CCATAAACCT CCCTGAGAAA ACAAGCTGGT CATGGCCTTG TGTAGTCTTG 1200 ACCTGTACTC CCCCATACCA ATTTAGTAGC TGATGAAGGA TTAACAAAGC ATCCATTTAA 1260
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