Tag | Content |
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EnhancerAtlas ID | HS133-13787 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr17:79622110-79623520 |
Target genes | Number: 53 | Name | Ensembl ID |
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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) |
HSF1 | MA0486.2 | chr17:79622694-79622707 | GAAAGTTCTGGAA | - | 6.29 | MYCN | MA0104.4 | chr17:79623260-79623272 | GCCCACGTGGCC | + | 6.27 | MYCN | MA0104.4 | chr17:79623260-79623272 | GCCCACGTGGCC | - | 6.27 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 3 | Chromosome | Start | End |
chr17 | 79622830 | 79623001 | chr17 | 79622555 | 79622720 | chr17 | 79622112 | 79623200 |
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Enhancer Sequence | GTTTATTGCT TTCTGCCTCT TGTCTGTGCT TTGCAGTTGG GGTGCTGTCA GTTCCCTTCA 60 CCCACTCACG GAGGCATCCC TGAGCCCCTC AGCACCATGA CGGGCACCCC GCAGTGCTGA 120 TGGAGAATGA CCCACAAAAT GGGGGGCAGG GTCCCCAGGC ACGGCGCCCC TGGGAAAGGG 180 GCCTGTCTCA GAGACTTGGT GCTGAGCTGT GAAGCCCTGC GTTCCCCAAC CCCACTTCAT 240 AGAGGGACAA GCTGGGGCTT GGGGACGGAG GGTGCCGGGC ATGTGTTCCC CCTGCTGGGG 300 GAATCACCAG GCCCTCTCTG TGTCTGGAGT CAGCTCGGGG AGCAGGGTCA CCCGCCTGGC 360 GTGGCGTGGC GTGGCTGAAG GGCCTCGGCC GCTCTGGACG AGATCAGTGT CCCTGCACTG 420 CTGCACAGGG TGGCCTCTCC TCCTCCTCTC CCTACAGCCT CTCCCCAGAT GCCCTAAGCC 480 CCAGTGACCT GGGCCAAGGG CAGTTCAGCT TCCCCTAAGC CTATTAACAG CAGAGGGGAA 540 TTCCTAATCT CCCATCGAGC TGCTGTCAGC TGCACATGCT GCCGGAAAGT TCTGGAAGGA 600 GGCACATGAC ACAGACAGGA GGGGCTGCTT GCCCGCACTG GATGCCCCAG GGACCACCTC 660 TTGGGGTCCC CTTTCCTGCC CCTGGTCTTT TTGGCTGGGA TTCCTGACTC CAGCCCTGGG 720 CTACTACCAG CTGTTTGCCG AGCTTCAGGC GTGAGAGTGA TCAGAAAGCA AGGGCAGGTG 780 GCCCATTTTG GGGACGCGGG CTCTGCAAGG GGTGCTGGGC ACCTGGGATT GGGGTGGACC 840 CTGCCATGGC ACCTTCCCTC ACTAAGGTTC AGCCTCTGTC CCCGGGACTG GGACCAGCAC 900 CAGCCTGTGC AAAACCAGCA CTCAGGAGCC CGGTGGTCCC AGCTGCTCAG ATCCCATGGC 960 ACCCAATCCT CATATCCTAG ATAGCACAGG CCCCGTCCAG CTGCTTCTCC AGCCCTGGGA 1020 CATGGGCTGT CCTGGGCAGC TCTGGGCCCT GATGGAGCTC CAACCATCAG ATGCCATCCA 1080 TGTGGAAACC GCTGCCTGCG CTGCCCTGGC CCGACCCAGC CTGTGACTGG CGTCCACTCA 1140 GGTCAGCTGA GCCCACGTGG CCTGAGGTTC CCAGACCATC ACTGGCCTGG GGATGGTGGA 1200 AGCACTGGTT ACCATGGGGG AGCAGAGGAG GAGGTTGGCT GGGAGTCCCC TCTGAATAAC 1260 AGGGTGGCGG GTAGGCATCT GCAGACCCAG ACCTCAGCCA CGGTGGTAAA AGCCTGTCAG 1320 CTCCCTCTGC CCCTTGGGTG ATGAGCAGAC CCCCACTGAC TCACTGGGGG AAGTGGCTGC 1380 CAGGAAAGAC AGCGGGGTTG GCCACTACTC 1410
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