Tag | Content |
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EnhancerAtlas ID | HS076-14959 |
Organism | Homo sapiens |
Tissue/cell | H1 |
Coordinate | chr12:117549140-117550070 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
MAFF | MA0495.3 | chr12:117549715-117549730 | ACGCTGACTCAGCAG | + | 7.13 | MAFF | MA0495.3 | chr12:117549715-117549730 | ACGCTGACTCAGCAG | - | 7.18 | NFE2L1 | MA0089.2 | chr12:117549716-117549731 | CGCTGACTCAGCAGA | + | 6.02 | Nfe2l2 | MA0150.2 | chr12:117549714-117549729 | CACGCTGACTCAGCA | + | 6.25 | ZNF263 | MA0528.1 | chr12:117549465-117549486 | CCTCCCTCCCCCACTTCCCTC | - | 6.13 |
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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: 2 | ID | Chromosome | Start | End |
GH12I117111 | chr12 | 117549361 | 117549550 | GH12I117112 | chr12 | 117549606 | 117550005 |
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Enhancer Sequence | GGATACCTGC AGGAACAGAC TCCACACTCA GGTGGAAGGA GGGGGATCCT TCCCAAAGGG 60 CCACCTCTGT GACCACAAAA GGGCACAGAC CGGGAGGAAA AGCTATGACT TAGCTGTCCC 120 CTCGGCTGTC TGGCCTCCAG GCAGGCCCAC ACCTCCAGTG TGCTAGTAAG TGACAGAGCT 180 GGAACTGAAT GCTGAGTTGG CCACCTTTGG GGGACCATGA GCTGCCCCAC GGGGCGATGC 240 AGCTGGCTGT GGAGCTGTGA GCCAATCTCA GCACCTCATT CACCCCGGCA CCTCCCCATC 300 CAGGGAGGCC CAGCCCCAGC CATCTCCTCC CTCCCCCACT TCCCTCCTGG GATGACTGCA 360 ATAACCAATG AGACCCGGCT GAGTGCCTGG GAGGCAGGGA TGATAAATAT ATGTTGGGGT 420 TCACAGTTGG TGCAGTTGAT AATTTGGGGC TTACTTGGGA AAGCAGGCAG CAGGCACCTA 480 CCATTTTGAC CGGCTGGGGC AGGCAGCCGG GGTGGGAGAC TGTAGAGGTA AGAGGTGGGG 540 CCTGGAGCCC TGAGGCCCCC CAGCCCTGCC TGGCCACGCT GACTCAGCAG AGCTCAGAAC 600 CTACTCTCCG CTGACAAGGC AAGCGTGCTC TTCCCAGCTG GCCGCTCTCA GCTGTCTCTT 660 CAAACCCTCC CAGGAGGGCT GCGGAGAGCA GACACGGGAA CCACACCTGG CTTCTTACCT 720 TCATGCAGGA AAACAAGGAG TGGGATGTGA ACAAAAGGCG GGAGGCTTCC CAGCTGCCCT 780 TTAAGTAGAA GCTTCATCTG TGCCAAGGAG ACCATGTGGT TAGTGGGTAG GGGAGAAAAA 840 TGCTTTGAGG GTTTCTGGGT CCCAGCTGCC TGCACAGGCG GGTGAAAGTC CTGCACCAGG 900 TTTGTTGTTT TGACCTGATA TAGGACCCTT 930
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