Tag | Content |
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EnhancerAtlas ID | HS133-12648 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr17:41161890-41163380 |
Target genes | Number: 34 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
MEF2A | MA0052.3 | chr17:41162688-41162700 | GCTAAAAATAGA | + | 6.92 | MEF2B | MA0660.1 | chr17:41162688-41162700 | GCTAAAAATAGA | + | 6.44 | MEF2C | MA0497.1 | chr17:41162686-41162701 | CTGCTAAAAATAGAA | + | 7.06 | POU4F2 | MA0683.1 | chr17:41162619-41162635 | ATGAATAACTAATGAT | + | 6.23 | Zfx | MA0146.2 | chr17:41163295-41163309 | GAGGCCGAGGCGGG | - | 6.01 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_35535 | chr17:41161771-41164515 | HepG2 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr17 | 41162878 | 41163074 | chr17 | 41162308 | 41162387 |
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| Number: 1 | ID | Chromosome | Start | End |
GH17I043010 | chr17 | 41162142 | 41164362 |
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Enhancer Sequence | AGCGAGCCGA TATTGCGCCA CTGCACTCCA GCCTAGGCAA CAGAGGGAGA CTCCGTCTCA 60 GAAAAGAAAA AAAAATAGAG GGCTGGGCGC GGTGTCTCAC ACCTGTAATC CCAGCACTTT 120 GGGAGGCTAA GACGGGCAGA TCATGAAGTC AGGAGATCGA GACCATCCTG GCTAACACGG 180 TGAAACCCCG TCTCTACTAA AAATACAAAA AAATTAGCCA GGCGTGGTGG CGGGCACCTG 240 TAGTCCCAGC TAATCGGGAG GCTGAGGCAG GAGAATGAAG TGAACTGGGA GGCGAAGCTT 300 GCAGTGAGCA GAGATCGCGC CACTGCACTC CAGCCTGGGC GACAGGGTGA GACTCCGTCC 360 CAAAAAGAAG AAAAAAAAAA AATAGCTGGC ATGATGGCAC ACGCCTGTAC TCAGGAGGCT 420 GAGATGAGAG GATTGATTGA TTCCAGGAGG TCGAGGCTGC AGTGAGCCAT AATGGAGCAA 480 TTGCACTCCA GCCTGGGTGG CATTGAGACT TTGTCTCAAA AAACAAAACA AAACAAAAAC 540 ATGGGTAGAT TTGCTGTGGG GGGAAACTTT GTTATGGCTA GAAGCAGTTT ACTTTAGAAA 600 GGACATGCTC TTCCCAGTGC GTCAGAGTCC CCACCACTCT CTGTTATCCT ACATGGCTCT 660 ATTAACTCAT TAATGTCATC CAACTGGCCC TTAAAGGCAC TGTGTTAGCA CTCTCTGAGT 720 TACAGAAATA TGAATAACTA ATGATCTTTT TCACTATTCA TAAACCAGCA TAATTTGGTC 780 AAGCTCTAGT ATTCTTCTGC TAAAAATAGA ACAAACTCAC ACTGAATTTC TTTGGTGTCC 840 TCTGTAATGT GCTCCTTTAC CGTCATTCAT TCACTTCATT TCTTCATTCA ACACAGTTTT 900 ACCGGACACA TATTTTGTGC CGGAGATCTT GCTGGACACA AGGAATACAG AGATGGTCAG 960 AACAGAGTCC TATCTTTCCA AGAGATCTCA TGCTTCTCTG AGCTGAACTT CTTTATCAGG 1020 ATTCCTAACC ACAGGGTGAA CTCTGCTCTA TTCCACAAAC AAAGGTGCAT TTATTGGTAT 1080 CCCTGGTGTC ACTTCCCTGC CTGTGATGTC AGTTCTCTCT CTGGACCCAT TCCAGATCAC 1140 ACCCAGCCTA AAAGGTTACT TGGTGTACAG TGGAAAGTGT GACAGTCCAG GGACAAGCTA 1200 GAATTGATGG GTAAACTACC TCCCCACTCT GGGCTTCATT TCTTCACTGT AAAGCACAGG 1260 TTAGTGGGTG GGCTCTGGAG TCAGACAGCC TAGGGCCAAA TGACTTTGGG CAAGTCATTT 1320 AACCTCTCTG AGCTTTAATT TCCTCATCTA TAAAATAAGG ATTGGCCAGG CATTGTGGCT 1380 TACACCTGTA ATCCTAGCAC TTTAGGAGGC CGAGGCGGGC AGATCATCTG AGGTCAGGAG 1440 TTTGAGACCA ACCTGGCCAA CATGGTGAAA ACCTGTTTCT ACTAAAAATA 1490
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