Tag | Content |
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EnhancerAtlas ID | HS176-08807 |
Organism | Homo sapiens |
Tissue/cell | SK-N-SH |
Coordinate | chr12:14986580-14987370 |
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 | CCTTAGGGTA TAAAGTCTGG AAGAAATACA TAATGATTAT AACTTTTATT TCATGAAGTC 60 TGAATCTGAA TTTTATCAGA CTGTTCAGAA GTAAATAGTC CTTAAACAGA AAAAGGTAAA 120 GCTGACGTGC AGTATACCAA GTCTAGTGTT TGAGGCAAAT GCTATCTATA GCCTCTTTCT 180 GTCAAAATGC AAGGAGCAAG AGTGTTAATA TTGTAGAATA TTACCTAGCA AAAACTTAGC 240 ACCCGAAAAT GAAAAGCGTT ATTCCTTCTG CCTCTTCCTT TGTTTCTCTT CTTACTATCA 300 ATTTCACTGA AGCACATGCT TGTGCCATTA AACCATTATC CCACTTCCAT GTGCAAAGTA 360 CTTTCCCAGA GTTTCTCAGT TGTGTTTGAA AGGAGGCAGA GACACCAATG CTATCACAAC 420 ATTCCCACAA GATGAGTATC ACTTCCATTT TATAAATGAA GAAACAGGCT CAGAGGTTAA 480 GTCATTTGCA CAAGGTCACC TAGCTACTAA CATATACCCA AATCTTTCTG GCTCCAAAGT 540 TTATTCACTT TCCACCATGC CGTGTGGTCT CCCAGATTTA TTCAATGACT CATTCTTTCA 600 TCCATTTATC TGAGACAGAC ACTCTACTTC AAGGTCATTG TGATGCCACA AATAGGGTAA 660 ACTAATTTTA GATAATTGAA GCCCAGAGTA AAAGAAAACA GGCAAAATAG AAAGCTAATA 720 AAATAAATAA TAATAATGAT AATAGTATCT TAAAAGTTTT GAGTACTTAA CATTTGTCAG 780 ATACTATTCT 790
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