Tag | Content |
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EnhancerAtlas ID | HS133-23763 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr4:7023440-7024530 |
Target genes | Number: 11 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ZNF263 | MA0528.1 | chr4:7023839-7023860 | GGAGGAGAGAATGGGAGAAGA | + | 6.28 |
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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 |
GH04I007019 | chr4 | 7021574 | 7025623 |
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Enhancer Sequence | ACCATTTTTG ATCTACAACG CAATAATATG CAGTGGTCGG AGGCAAAACG TAAACATCTT 60 TTGGGAGAGA AAAACCCTTG AATTCTGTCT TCCGACCATG GGAGGAGTAC TGAGCCGTCT 120 CTGGGAAGGC CAAGGGGCCC TTCCCGTCCT GCTTCTGTGA GCCTGAGGGC AGCAGGGGAA 180 GGTGGACCTT GAACCAGGAG GGCCGTGTGG ACAGTAGCCC CCTTGTTCCG ACCGGTTCTG 240 ATCCCATGGC AGGGCTTCTT TGGGGCCAGG ACAGAGCCTG GTGTCCCCCT TCAGTGGCCT 300 GTTCACGGCT GGCTTTCAAA TCTAAATGTG GTTTAAAATA AAGCCCACAT TTGGAAGCTC 360 CTGATAATGA TGTGGGAGCA CCTCTGAGCA GTCCCTGCTG GAGGAGAGAA TGGGAGAAGA 420 GGAGCCTCAG TTCAAGACTG TGGGGCGGGG TCTCTGCCCT TGAGGCACTT CCAGCCTGGA 480 GCAGGGGACA GAAGTGGCTT AGGACGGTGC AGAGCTCTTG GAGTGGAGTC CAGGGGCTGG 540 AGAGGCCATG GGGAGCCCTG ACTGGGGCAG AGGGCCTGGG AGCTGCTTGC TGAGAGGCCT 600 GCCAGAGCCT GCAAGGCCCA AAAGATGCAG GATGGTATGC GAGGCAGAGG GAAGTGTCCA 660 GGAGTGTCAG GAGCGTCCCT TCACTGACTC AGTGTAAAGG AAGGTGAAGA ATGCCAGGGC 720 CTCATGAAGG AGGGTGCGTG CAGTGCAGCG TGAACATTTC AAGGAAACTT GGTCCAGCCT 780 GAGGGTCAGG AAATGACCTT CCAAGAAATA GTGACACACA GCATGTGGGA AGAGCCTGCA 840 GGGGACAGAG GCTGATGCCA GGAACAAGCC CAGAGGCCGC AGTGAGTAGC CAGGCATGGT 900 CGCAGCACGG CGTCAGCAGT AAGCATGGCC AGGAGGTGGA AGCTCATGGG ATTGGAAATG 960 GATTTGTCTC ATGGAAATGC AGAGCAGGGG GCATCGTGGG CATAGTGAAT GGCATTCTGG 1020 GTCATTCCAG TGGTGACTTA ATTTTATAAA GTTCATTACC TGTCTAGAGT AACTTATGGA 1080 GACTCACACA 1090
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