Tag | Content |
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EnhancerAtlas ID | HS133-10291 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr15:72650510-72651990 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOSL1 | MA0477.1 | chr15:72651026-72651037 | AGTGACTCATC | + | 6.02 | JUND | MA0491.1 | chr15:72651026-72651037 | AGTGACTCATC | + | 6.32 | Six3 | MA0631.1 | chr15:72651171-72651188 | AATAGGGTATCACCACT | + | 8.33 |
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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 |
GH15I072358 | chr15 | 72650498 | 72652665 |
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Enhancer Sequence | ACCCCATCCT CTGACTTCTT GCCCCCACTC CCAACCCCAC ACATCATGGA GCCCCAATAT 60 CATTGTGTGG AGAATTCATC TGCATATCTA CCCAGGCAGC CATCCAAAAG ACAGCCGAAG 120 TCCTGAGCTT TAGTTCTAAT CCTCTGGGGC TCAGCCTGCC ACATAAGGAG AAATCACAAC 180 TAATCCATAT GCAACTACCA TGGCTCGCTG CCCTCATGAC AAAATAAGAG AGGCCACACA 240 AACACCAGGT TTATCTGAAC TATTACTTGG AAGACAGAAA AATACCTAAT CTTTCGATTT 300 TTAAAAAATT TATTTTTCTA AAAGACACCT GCACTGTACT CCCTAAATCT GTAGTCTTTT 360 GGAGAGTCAC AGACTCCTTT GCAGATCTGC TGAATAGGAA AACACTTTTT TTCCCAGAAC 420 AATGCCCCTA ATTTAAGGGC TGTTTCTCCA GAATTACAAT TCTTCCACTC CCTGCCATCA 480 ATCTCATGGT GAAGAATCCC TGTCCGAAGT TCTCTCAGTG ACTCATCTGG GTTTGGGCTG 540 AAAGAAGTAG ATACGGGGGC ATGGCTGCTG TTTAAACAAA TTATGAGAGG GATGTTTGGG 600 GGAGGCAGCA ACATGAGAGC TGGCAAAACA GGAGGGACAC TAGGTCATTG TAAAGGATGT 660 AAATAGGGTA TCACCACTGT GGTTTTCCGC CTCCAAGTTG CTACTTTGCC TGGCTATGAA 720 GAGGGCAGGA AATAGGCAGG GGACAGTAGT ACAGCCGCCT CTACACACAC CCGCCCACAC 780 CCTGAACACT GAGAAGCACC AACGTGTGGG AAGCACAGTA TGGCAAACAG CCCGGTCAGC 840 CAGCAATGTC ATGAGCACAT GTGCCATGAG TCTGGCTGGA ACAGCAGGAA ATTGAGAAGC 900 CTCCAGGGCT TAGGAGGTAG CATGAAAAAC AGACCAGAGG GCTGGGAAAT CAGGACAGGT 960 TGCTTCTGGT TCTGGTTTTG CTGCTGCCAA GCTGAGCAAG TCTCAGGGCT CCCATTTCCT 1020 TCCCTGTAAA CAATGGCAGG GTGGGACCAG ATTCCAGCTA CTCCTCTTCA GATCTAAGAC 1080 CTTGTGATTC CATAGACAGA TAATACACTC CAGGGTCCCA TTCCAGGACC ACAGCCTGCT 1140 ACCTCTGCAG CTCACTCATC TCCCTGCTTT CATGTAAACC TACTCTTCTC TTTGGGTTCA 1200 CTGAAAACTT TGTATCTTTT TTTAAAATCA AAACAGTTGT ATAGGCCTGG TGCGGTGGCT 1260 CAGGTCCATG ATCTCAGCAC TTTGGGAGGC TGAGGCAGGC GGATCACTTA AGGTCGGGAG 1320 TTAGTGACCA GCCTGGCCAA CACGGTGAGA CCCTGTCTCT ACTAAAAATA CAAACAAATT 1380 AGCTGGTCAT GGTGGTGGGC CCTGTAATCC CAGCTACTCA GGAGGCTGAG GCAGGAGAAT 1440 CACTTGAACC CAAGAGACGG AGGCTACAGT GAGCAGAGAC 1480
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