Tag | Content |
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EnhancerAtlas ID | HS098-14488 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr12:109995500-109996900 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ZNF263 | MA0528.1 | chr12:109995641-109995662 | CCCTTTCCCGCCTCCTCCTTT | - | 6.16 | 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: 4 | Chromosome | Start | End |
chr12 | 109996291 | 109996413 | chr12 | 109995950 | 109995998 | chr12 | 109996468 | 109996742 | chr12 | 109995574 | 109995936 |
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| Number: 1 | ID | Chromosome | Start | End |
GH12I109558 | chr12 | 109996032 | 109997016 |
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Enhancer Sequence | CTGACAGCAC CTTTGGTCTC CACCCACCAG GTGCCAGTGG CACCCCTGCA CCCAGTGTGA 60 CAACTAGTAA TGCCTCCAAA CATCGCCAAA GGTACCGGGT GAGAAGCACA GGCTGGAGCA 120 CTCTAGAGAC CAGAGCCCAG CCCCTTTCCC GCCTCCTCCT TTGAACCAAC AGCAATGGTC 180 ATCTGTGCAT GAGGCCTTCT GCAGGGGCAG CAGTGGAGGG AACTAGAGGA CGACGCCACG 240 GGCCCCAGAA GGCGCTTACG CTGTCAGCTC TTCTGCCTTC TGCTGTCCGC ACCTTTTGCT 300 GTTTCACTCC CAGCACGAGG CACCACGTTC CTCCCTCTCT CTCTGCCCCA GTCTTGCCCT 360 CAGAGGCCAG CTCCACACCA CATCCTCCTG AGTCCTCCCC TGACTCAGGC CCCCTGGGCC 420 CCACGGCTGG CTCTCAGGAA GAGCGAAGGG GAGGTTGTTC AGGGTATTTT ACCCCTGGGC 480 CGCATGCTCC TGGAGGGCAG TGGTGTGCCT GTTGCTTGTT GGCTCTGTGA AGCCTCACTG 540 AGGAGATGAA ATGGCCTGTC CCGTGCAATG CTATGGGACC GCAGGGTTGC TGCTTTGAAG 600 GTGAAGTAGA CCTGCTCCTC ACTCCCGGCG AAACCCCCCT CCCAGAAGGA AAGGAGCTGC 660 TCAGGACCCG TCAAAGCGCC ATGTCTCTGG GAGGAGTGGC CACAGTCAAG GGCCTGAGGT 720 CACTTTCTAG ACACCCAGGA CAGCTCCTGG GGTGCAGACC TGCTCCCCCA GCTCTCTACC 780 TGCCCCCAGG CTCTGGCCTT GCCCACACTG ATGCCACAGA AGCCAGGGCT GGGGCAGGAA 840 CCCGCAGAGC AGGCTTTGGG CCAGGTGTGG CTCCAGCCTC ATGGGCCGGC CGCGAGGCAG 900 AGGAAGCCCT CCCTGGGCTA GCCTGGCTCA CTGGGGCCTG CATGGGGTCC CCTGAGCGCA 960 GCTTGGCCCG GCTCTCTTGT TGGTTCATGC TGCCGCAGGC CCTCTCGGGG ACAGGAAACT 1020 GGCTGAGAGA GGGCCTGAAG CCTGGCTCCC TGGTCAGTCA CCACCGAGAG GCCTCCCCTG 1080 AGCACCCAGC CTCTAAGAAC GCCCTTTGCC CCCGCAATGC CACTTTGCAC TTAGGTTTTT 1140 CTTCCTGGTT TTTACAGCAG CCTCTCCCAA TAAGATCTAA ATCTTATCGG GACAGGCACA 1200 GGGCCCACCT TGTTCACCAC TGCCTCCCCT GTGCCCGGCG TGGTGCCTGG CACAGAGCAG 1260 ATGTTCATAA ACACTAAGGG AATGAAGGAG GGGGTGCGGG AATGCTGCCC CACACTGCTT 1320 CCCGGACCGC TGCACCGCTG CTACTTCCCA CAGATGAGCC TCGGCTTTCA GAGAGGAACC 1380 CCCAGGTTCC ACGCGAGTAC 1400
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