Tag | Content |
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EnhancerAtlas ID | HS104-15558 |
Organism | Homo sapiens |
Tissue/cell | HUVEC |
Coordinate | chr12:109995450-109996710 |
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: 3 | Chromosome | Start | End |
chr12 | 109996291 | 109996413 | chr12 | 109995950 | 109995998 | chr12 | 109995574 | 109995936 |
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| Number: 1 | ID | Chromosome | Start | End |
GH12I109558 | chr12 | 109996032 | 109997016 |
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Enhancer Sequence | TCATTCTGTG TGTTCGGGGC TGTCCTGTGC ATCCTGTGCA GTGTAGGATG CTGACAGCAC 60 CTTTGGTCTC CACCCACCAG GTGCCAGTGG CACCCCTGCA CCCAGTGTGA CAACTAGTAA 120 TGCCTCCAAA CATCGCCAAA GGTACCGGGT GAGAAGCACA GGCTGGAGCA CTCTAGAGAC 180 CAGAGCCCAG CCCCTTTCCC GCCTCCTCCT TTGAACCAAC AGCAATGGTC ATCTGTGCAT 240 GAGGCCTTCT GCAGGGGCAG CAGTGGAGGG AACTAGAGGA CGACGCCACG GGCCCCAGAA 300 GGCGCTTACG CTGTCAGCTC TTCTGCCTTC TGCTGTCCGC ACCTTTTGCT GTTTCACTCC 360 CAGCACGAGG CACCACGTTC CTCCCTCTCT CTCTGCCCCA GTCTTGCCCT CAGAGGCCAG 420 CTCCACACCA CATCCTCCTG AGTCCTCCCC TGACTCAGGC CCCCTGGGCC CCACGGCTGG 480 CTCTCAGGAA GAGCGAAGGG GAGGTTGTTC AGGGTATTTT ACCCCTGGGC CGCATGCTCC 540 TGGAGGGCAG TGGTGTGCCT GTTGCTTGTT GGCTCTGTGA AGCCTCACTG AGGAGATGAA 600 ATGGCCTGTC CCGTGCAATG CTATGGGACC GCAGGGTTGC TGCTTTGAAG GTGAAGTAGA 660 CCTGCTCCTC ACTCCCGGCG AAACCCCCCT CCCAGAAGGA AAGGAGCTGC TCAGGACCCG 720 TCAAAGCGCC ATGTCTCTGG GAGGAGTGGC CACAGTCAAG GGCCTGAGGT CACTTTCTAG 780 ACACCCAGGA CAGCTCCTGG GGTGCAGACC TGCTCCCCCA GCTCTCTACC TGCCCCCAGG 840 CTCTGGCCTT GCCCACACTG ATGCCACAGA AGCCAGGGCT GGGGCAGGAA CCCGCAGAGC 900 AGGCTTTGGG CCAGGTGTGG CTCCAGCCTC ATGGGCCGGC CGCGAGGCAG AGGAAGCCCT 960 CCCTGGGCTA GCCTGGCTCA CTGGGGCCTG CATGGGGTCC CCTGAGCGCA GCTTGGCCCG 1020 GCTCTCTTGT TGGTTCATGC TGCCGCAGGC CCTCTCGGGG ACAGGAAACT GGCTGAGAGA 1080 GGGCCTGAAG CCTGGCTCCC TGGTCAGTCA CCACCGAGAG GCCTCCCCTG AGCACCCAGC 1140 CTCTAAGAAC GCCCTTTGCC CCCGCAATGC CACTTTGCAC TTAGGTTTTT CTTCCTGGTT 1200 TTTACAGCAG CCTCTCCCAA TAAGATCTAA ATCTTATCGG GACAGGCACA GGGCCCACCT 1260
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