Tag | Content |
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EnhancerAtlas ID | HS105-20379 |
Organism | Homo sapiens |
Tissue/cell | IMR90 |
Coordinate | chr12:109995800-109996670 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ZNF263 | MA0528.1 | chr12:109995828-109995849 | TCCTCCCTCTCTCTCTGCCCC | - | 6.31 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr12 | 109996291 | 109996413 | chr12 | 109995950 | 109995998 |
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| Number: 1 | ID | Chromosome | Start | End |
GH12I109558 | chr12 | 109996032 | 109997016 |
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Enhancer Sequence | GTTTCACTCC CAGCACGAGG CACCACGTTC CTCCCTCTCT CTCTGCCCCA GTCTTGCCCT 60 CAGAGGCCAG CTCCACACCA CATCCTCCTG AGTCCTCCCC TGACTCAGGC CCCCTGGGCC 120 CCACGGCTGG CTCTCAGGAA GAGCGAAGGG GAGGTTGTTC AGGGTATTTT ACCCCTGGGC 180 CGCATGCTCC TGGAGGGCAG TGGTGTGCCT GTTGCTTGTT GGCTCTGTGA AGCCTCACTG 240 AGGAGATGAA ATGGCCTGTC CCGTGCAATG CTATGGGACC GCAGGGTTGC TGCTTTGAAG 300 GTGAAGTAGA CCTGCTCCTC ACTCCCGGCG AAACCCCCCT CCCAGAAGGA AAGGAGCTGC 360 TCAGGACCCG TCAAAGCGCC ATGTCTCTGG GAGGAGTGGC CACAGTCAAG GGCCTGAGGT 420 CACTTTCTAG ACACCCAGGA CAGCTCCTGG GGTGCAGACC TGCTCCCCCA GCTCTCTACC 480 TGCCCCCAGG CTCTGGCCTT GCCCACACTG ATGCCACAGA AGCCAGGGCT GGGGCAGGAA 540 CCCGCAGAGC AGGCTTTGGG CCAGGTGTGG CTCCAGCCTC ATGGGCCGGC CGCGAGGCAG 600 AGGAAGCCCT CCCTGGGCTA GCCTGGCTCA CTGGGGCCTG CATGGGGTCC CCTGAGCGCA 660 GCTTGGCCCG GCTCTCTTGT TGGTTCATGC TGCCGCAGGC CCTCTCGGGG ACAGGAAACT 720 GGCTGAGAGA GGGCCTGAAG CCTGGCTCCC TGGTCAGTCA CCACCGAGAG GCCTCCCCTG 780 AGCACCCAGC CTCTAAGAAC GCCCTTTGCC CCCGCAATGC CACTTTGCAC TTAGGTTTTT 840 CTTCCTGGTT TTTACAGCAG CCTCTCCCAA 870
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