Tag | Content |
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EnhancerAtlas ID | HS175-12836 |
Organism | Homo sapiens |
Tissue/cell | SK-N-MC |
Coordinate | chr19:5563880-5564510 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EHF | MA0598.2 | chr19:5564179-5564191 | TACCCGGAAGTG | + | 6.37 | ELF1 | MA0473.2 | chr19:5564179-5564191 | TACCCGGAAGTG | + | 6.62 | ELF3 | MA0640.1 | chr19:5564179-5564192 | TACCCGGAAGTGA | + | 7.04 | ELF4 | MA0641.1 | chr19:5564179-5564191 | TACCCGGAAGTG | + | 6.74 | ELF5 | MA0136.2 | chr19:5564180-5564191 | ACCCGGAAGTG | + | 6.32 | ZBTB7A | MA0750.2 | chr19:5564180-5564193 | ACCCGGAAGTGAG | + | 6.15 | ZNF263 | MA0528.1 | chr19:5564152-5564173 | GGGGGAGGGAGAAGAGGGGGC | + | 7.44 |
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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 |
GH19I005563 | chr19 | 5563052 | 5565360 |
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Enhancer Sequence | GCGCCACTGC ACTCCAGCCT GGGCGACAGA GCAAGACTCC CGTCTCAAAA ATAATAAATA 60 ATAAATAAAT AAAAGCATCC TCGCCAGGGG ACAGCGGTAA GGCCACGTGA AAAGCCCCTA 120 GCATCTCAAA GGCTCTCAAA GCATGACCAT GACTCAGTGC CTGCTAGCTC CCGTGACAAC 180 CTGTCTCCCT GCAACGCTGC TGCCTCGAGG CAGAAAATGT TGTCACTACT GCATTTCACA 240 GAGTGTAGAA ACAGGAGGTG GCAAGAGAGG CTGGGGGAGG GAGAAGAGGG GGCCCTATCT 300 ACCCGGAAGT GAGAGAGGGC CTGGCAGGTT TGTCCCGAGC AGCCCACGCA GCTTCTCTCT 360 CCCTAGGGTA CCGTCTGCGC TGACAGGTCC CAAGTGTTTT TCTCATTTCT CACATGGGGA 420 AGCTGAGGCC TCCCCGGCTG CTGCTGCACC ATCCACTAGT AGCCCCTGCT CTGCCTCTAG 480 AGGTCTGGGA GTGGTCTGGG GAGCTCAGAA CCCATTTGAT GCCCAGAGAG GGTGGGTTAG 540 CTGCCTCGGG ACACACAGCC AGTGAACAGC AAAGGCAGAT AGGGGCCCCT GTCTGTTGGG 600 GAAGACAAAG CTGGACTCTG CCATCAACCC 630
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