Tag | Content |
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EnhancerAtlas ID | HS174-05290 |
Organism | Homo sapiens |
Tissue/cell | SK-MEL-5 |
Coordinate | chr6:3955660-3957150 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Nr2f6(var.2) | MA0728.1 | chr6:3955989-3956004 | TGAACTCCTGACCTC | - | 6.22 | PHOX2A | MA0713.1 | chr6:3957038-3957049 | TAATCTAATTA | + | 6.32 | PROP1 | MA0715.1 | chr6:3957038-3957049 | TAATCTAATTA | + | 6.14 | Phox2b | MA0681.1 | chr6:3957038-3957049 | TAATCTAATTA | + | 6.32 |
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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 |
GH06I003956 | chr6 | 3956401 | 3956550 |
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Enhancer Sequence | CCATGTTGGC CATGCTAGTC TCGAACTCCT GACCTCCGAT GATCCACCCG CTTTGGCCTC 60 CCAAAGTGCT GGGCTTACAG GCATGAGCCA CCGTGCCCGG CTTACAATAC TTTTTTTTTT 120 TTTTTTTGAG ACAGAGTATC ACTCTGTCGC CTAGGCTGGG GTGCAGTGGC GCGATCTCGA 180 CTCACTGCAA TATCTGCTTC CCGGGTTCAA GCAATTTTCC TGCCTCAGCC TTTTGAGAAG 240 CTGGGATTGC AGGCGCCCAC CACCATGCCC GTCTAATTTT TGTGTCTTTT AGTAGGGATG 300 AGTTTTCACC ATGTTGGCCA GGCTGGTCTT GAACTCCTGA CCTCACGTGA TCAGCCCACC 360 TCAGCCTCTC AAAGTGCTGG GATTACAGGC ATGAGCCACC GGCCAATACT TTCTTTGTCA 420 TAGATCACAT ACCTACATAT GTGTGGCTCT GTTTTTGGAC TTTGATTTTT CCATTGCTCT 480 CTTTTCTATT CTTGTTTCAA TGTTACTGTG TTAATTCTTG TGGCTTTATA TTAAGTCTTA 540 GTTTCTCTCG AGTGCTTTAT TTTTTAGTTC TTTAAGGATG TCTTGGCTTT TCTTGGCCTT 600 TTGCGTCTTG CATAAATTTT AGAATCAGGT TGCTAATTTG CTGAGAGTAG CAAGAAGGAG 660 TGCCCCATTC ATGGCCTTGT ACTTTGAGGA TTTTAATGGG TTGCAAGGAA CTCATTTTGT 720 GAGCAGCGAT GAATCTGCTT CAGATAAAGT AAATCAGAGC TGGAGGTAGG GCAGGGTTCT 780 TCATGCTAGC CTGGGGCTGC ATAACTCAAT GAACACTGGC TGAGGCAACA ATGGGTCTTT 840 TGTGATGAAA CTGGTACCTA CTCAGGCTAT GGGGCCTGAG GTTTCATCAT ACATCATTGG 900 GTTTATTAAA GCTTAAAAGT GATCTAATAA TTAACATGCC AGCTACTAGT TATTTGTTGA 960 GTTTTTTTCC TTTTTAGTCA GGGAAAATGA GAGTGAGGGA AAAGGAAAAG GAAGCAACCC 1020 TAAGGGGCAA CAAGACCATT AATTATTACA AATATCAATA GGACACAAAT GACCCTTTGT 1080 CTCTCAGGCT GGAGTGCGGT GGCGCGATCA CAGCTCACTG CAGCCTCGAC TTCCCAGTCT 1140 CAAATGATCC TCCTACCTCA GCCTCCTGAG TAGCTGGGAC CACAGGTGCA CATCATTATG 1200 CCCTACCAAT TTTTAAATTT GTTATAGAGA TGAGGTCTCC CTATGTTTGC CAGGCTGGTC 1260 TTGAACTCCT GGCCTCAAGT GATCTCCTGC CTTGGCCTCC CAAAGTGCTG AGATTACAGG 1320 CATGAGCCAC TACACCTGAC CCAAATGGGT AATTTAGTTG CATAAGGTCT TTCCTTCATA 1380 ATCTAATTAG AAAACTTTGG GGCAGGACTC CAAGGCTTAC TTTTGACCCT CATTCCACTC 1440 CTGCCCTACT CTTCATTGTT CTAAAAAATG GAAAAACAGG TTGATTACAT 1490
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