Tag | Content |
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EnhancerAtlas ID | HS092-11359 |
Organism | Homo sapiens |
Tissue/cell | HFF |
Coordinate | chr12:14986570-14987320 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ESRRB | MA0141.3 | chr12:14987208-14987219 | TCAAGGTCATT | + | 6.32 | Esrra | MA0592.2 | chr12:14987207-14987218 | TTCAAGGTCAT | + | 6.62 | Esrrg | MA0643.1 | chr12:14987208-14987218 | TCAAGGTCAT | + | 6.02 | JUN(var.2) | MA0489.1 | chr12:14987164-14987178 | ATGACTCATTCTTT | - | 6.6 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| Number: 1 | ID | Chromosome | Start | End |
GH12I014834 | chr12 | 14986938 | 14991193 |
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Enhancer Sequence | GTCATCTCTG CCTTAGGGTA TAAAGTCTGG AAGAAATACA TAATGATTAT AACTTTTATT 60 TCATGAAGTC TGAATCTGAA TTTTATCAGA CTGTTCAGAA GTAAATAGTC CTTAAACAGA 120 AAAAGGTAAA GCTGACGTGC AGTATACCAA GTCTAGTGTT TGAGGCAAAT GCTATCTATA 180 GCCTCTTTCT GTCAAAATGC AAGGAGCAAG AGTGTTAATA TTGTAGAATA TTACCTAGCA 240 AAAACTTAGC ACCCGAAAAT GAAAAGCGTT ATTCCTTCTG CCTCTTCCTT TGTTTCTCTT 300 CTTACTATCA ATTTCACTGA AGCACATGCT TGTGCCATTA AACCATTATC CCACTTCCAT 360 GTGCAAAGTA CTTTCCCAGA GTTTCTCAGT TGTGTTTGAA AGGAGGCAGA GACACCAATG 420 CTATCACAAC ATTCCCACAA GATGAGTATC ACTTCCATTT TATAAATGAA GAAACAGGCT 480 CAGAGGTTAA GTCATTTGCA CAAGGTCACC TAGCTACTAA CATATACCCA AATCTTTCTG 540 GCTCCAAAGT TTATTCACTT TCCACCATGC CGTGTGGTCT CCCAGATTTA TTCAATGACT 600 CATTCTTTCA TCCATTTATC TGAGACAGAC ACTCTACTTC AAGGTCATTG TGATGCCACA 660 AATAGGGTAA ACTAATTTTA GATAATTGAA GCCCAGAGTA AAAGAAAACA GGCAAAATAG 720 AAAGCTAATA AAATAAATAA TAATAATGAT 750
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