Tag | Content |
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EnhancerAtlas ID | HS133-26718 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr6:31878750-31880270 |
Target genes | Number: 41 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
IRF1 | MA0050.2 | chr6:31879395-31879416 | TGTTTCTTTCTTTTTTTTTTT | + | 6.2 | SNAI2 | MA0745.2 | chr6:31879963-31879973 | TGCACCTGTT | - | 6.02 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 4 | Chromosome | Start | End |
chr6 | 31880093 | 31880215 | chr6 | 31878758 | 31879525 | chr6 | 31879137 | 31879421 | chr6 | 31879746 | 31879796 |
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| Number: 1 | ID | Chromosome | Start | End |
GH06I031910 | chr6 | 31877939 | 31879970 |
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Enhancer Sequence | CATCTTAAAA ATAAAATAAA AAATAAATAA ATAAAATGAA TTGGGCTGGG TGTGGTGGCT 60 CATGCCTGTA ATCCCAGCAC TTTGGGAGAC CAAAGCGGGT GGATCACCTG AAGTCAGGAG 120 TTCGAGACCA GCCTGAGCAA CAAGGTGAAA CCCCGTCTCT ACTAAAAATA CGAAAATTAG 180 CCAGACGTGG TGGCAGGCAC CTGTAGTCCC AGCTACTCGA GAGGTGGAGG CAGGAGAATT 240 GCTGGAACCT GGGAGGCGGA GGTTGCAGTG AGCCGAGATG GCGCCACTGC ACTCCAGCCT 300 AGGAGACAGA GGGAGACTCT TGTCTCAAAA AATAAACAAA TAAATACATA AAAAAAAAAA 360 TAAAATGAAT CATGAAGGGA ATGGTTAAAA AGTGAAATAA GACTTTTAAA AAAAGATCCA 420 TGTTTACAAC ACACTGGAAT GGCATTCTTT TGCAACTAAA CATTTGGGGA AAGTTTTAGA 480 TAGCAGCATA AAAACATGCA AGGGGTACAT AATTTGCAAA ATTCTTTTAA TGTGAGCAAA 540 AGGGTTTGAA GATTACATGC TTCTTGAAAT CAGCATGCAC ATGAGTCATC TGGAGTTTTA 600 ATTCGGAGTC TGAGTCAGTA GGTCTGGGTG GGGCCTGAGA TTCTGTGTTT CTTTCTTTTT 660 TTTTTTTTCT CTCTCTTTTT TTTTTGAGAC AGAGTCTCGC TCTGTTGCCC AGGCTGGAGT 720 GCAGTGGCAC ACTGCAGCCT CCGCCTCCCG GGTTCAAGCA ATTCTCCTGC CTCAGCCTCC 780 CAAGTAGCTG GGACTACAGG CACATGCCAC CACGCCTGGC TAATTTTTGT ATTTTTAGTA 840 GAAATGGGGT TTCACCATGT TGGCCAAGCT GGTCTCGCAC TCCTGACCTC AGGTGATTTG 900 CCCGCCTCAG CCTCCCAAAG TGCTGAGATT ACAGGCATGA GCCACCATGT CTGGCCCTTT 960 TTTTTTTTTT TTTTTTCCAA TTTGAGACCG GGTCACTACG TTGCCAAGGC TGGTCTCTAA 1020 CTCCTGGGCT CAAGCGATCC GCCCACTGCA GTCTCCCAAA GTGCTGGGAT TACAGGCGTT 1080 GAGCCACCGT GCCTGGCCAG ATTCTGCATT TCTACAAGTT CCTGCTGATG CTGATGCTGT 1140 CTGTCTGTGG ACCACAGTCT GAGTAGCAAG CATCCACATA TTCGTAAGAG TGGAGTTGCT 1200 GGATGTTGAG GTCTGCACCT GTTCAGCTTC CCTGCTAATG CTAAACTATT TTCTGAAGCA 1260 GTTGTACACC AGCCATGAGA CTGTTGCTTC TTGGGAAAAA AGATATAAAG GCTTCAAATT 1320 TAATGGATAT TATTCAGTGC TCCTCTTACT TGAGCTTTCT GCAGTCTGTG ACATACTTGA 1380 CCACACTGTT TGATCCACTG CTTTTCCCTG GTTTCCATGA CACCCCTGTA TCCAGGCTCC 1440 CTTCCTTCTA TAATTTCAGT CTGTTCTATA AACCCTCACT CCTTTCCTGT CTTGACCTTT 1500 TCCTCTGTTG ATGCCTTTGG 1520
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