Tag | Content |
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EnhancerAtlas ID | HS098-14779 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr12:122072150-122073140 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ZNF263 | MA0528.1 | chr12:122072641-122072662 | GGGAGAGGGAGAGGGAGAGGG | + | 6.44 | ZNF263 | MA0528.1 | chr12:122072632-122072653 | GGAGGGGGAGGGAGAGGGAGA | + | 6.53 | ZNF263 | MA0528.1 | chr12:122072639-122072660 | GAGGGAGAGGGAGAGGGAGAG | + | 6.5 | ZNF263 | MA0528.1 | chr12:122072623-122072644 | TGGGGAGAGGGAGGGGGAGGG | + | 6.77 | ZNF263 | MA0528.1 | chr12:122072629-122072650 | GAGGGAGGGGGAGGGAGAGGG | + | 8.08 | ZNF263 | MA0528.1 | chr12:122072635-122072656 | GGGGGAGGGAGAGGGAGAGGG | + | 8.44 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_22457 | chr12:122072473-122073347 | CD8_primiary |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr12 | 122072659 | 122073097 | chr12 | 122072444 | 122072494 |
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| Number: 1 | ID | Chromosome | Start | End |
GH12I121634 | chr12 | 122072474 | 122073347 |
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Enhancer Sequence | CCTCACTTCC CAGTAGGGGC GGCCAGGCAG AGGCGCCCCG CACCTCCCGG ACGGGGCGGC 60 TGGCCGGGCA GAGGCTGCAA TCTCGGCACT TTGGGAGGCC AAGGCAGGCG GCTGGGAGGT 120 GGATGTTGTA GCGAGCCGAG ATCACGCCAC TGCACTCCAG CCTGGGCACC ATTGAGCACT 180 GAGTGAAGGA GACTCCGTCT GCAATCCCGG CACCTCGGGA GGCCGAGGCT GGCGGATCAC 240 TCGCGGTTAG GAGCTGGAGA CCAGCCCGGC CAACACAGCG AAACCCCGTC TCCACCCAAA 300 AGATACGAAA ACCAGTCAGG CGTGGCGGCG CACGCCTGCA ATCGCAGGCA CTCGGCAGGC 360 TGAGGCAGGA GAATCAGGCA GGGAGGCTGC AGTGAGCTGA GATGGCAGCA GTACAGTCCA 420 GCTTCGGCTC GGCATCAGAG GGAGACTGTG GAAAGAGAGG GAGAGGGAGA CTGTGGGGAG 480 AGGGAGGGGG AGGGAGAGGG AGAGGGAGAG GGCCTTTCTT CTCACTTTGA ATCATTCTTT 540 TACACGGCCC CCTGAACCCT GTGGCATTGA ACTTGGTTCC AAGTGTGGGC ACATACAGCC 600 TGCCTAAGTG GACGGAGTTC CAGGAATCGT AGGGTCTGGT GAGGGTAATG GGCTTTCTTC 660 CGGAGCAGGG CAGCAGGCCC TTTCCTCTTC CTCGGAGAGC CCAGCCTCTC CCCTCTCCCC 720 AGCCCAAAAC CTCAGGGCTG GCGAGTGTGG GTGTCCCCGG GCCGTGTGCG TCCCAACAGC 780 TGCACTGCTT TCTGGCCCTG GAGCCTGTGG GTGTGACAAA TGGTGTGGAA TGTGGTGGTC 840 TCTGTCCTGT GGAGGTGGCC ATCAGGCCAG GTGTGGCGTG GGGTACACAT CCTTGTGGCC 900 GAGGTTTGGA GCTGGAGCTG CCTCTAAATA TAGCAAGCGA GGCCCCGAGT CGGGGTTGGA 960 AGGTGGGTAT GTGGGGTCCC TGTCTCCAGT 990
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