Tag | Content |
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EnhancerAtlas ID | HS089-03691 |
Organism | Homo sapiens |
Tissue/cell | Hela |
Coordinate | chr12:122072250-122073020 |
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: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH12I121634 | chr12 | 122072474 | 122073347 |
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Enhancer Sequence | AAGGCAGGCG GCTGGGAGGT GGATGTTGTA GCGAGCCGAG ATCACGCCAC TGCACTCCAG 60 CCTGGGCACC ATTGAGCACT GAGTGAAGGA GACTCCGTCT GCAATCCCGG CACCTCGGGA 120 GGCCGAGGCT GGCGGATCAC TCGCGGTTAG GAGCTGGAGA CCAGCCCGGC CAACACAGCG 180 AAACCCCGTC TCCACCCAAA AGATACGAAA ACCAGTCAGG CGTGGCGGCG CACGCCTGCA 240 ATCGCAGGCA CTCGGCAGGC TGAGGCAGGA GAATCAGGCA GGGAGGCTGC AGTGAGCTGA 300 GATGGCAGCA GTACAGTCCA GCTTCGGCTC GGCATCAGAG GGAGACTGTG GAAAGAGAGG 360 GAGAGGGAGA CTGTGGGGAG AGGGAGGGGG AGGGAGAGGG AGAGGGAGAG GGCCTTTCTT 420 CTCACTTTGA ATCATTCTTT TACACGGCCC CCTGAACCCT GTGGCATTGA ACTTGGTTCC 480 AAGTGTGGGC ACATACAGCC TGCCTAAGTG GACGGAGTTC CAGGAATCGT AGGGTCTGGT 540 GAGGGTAATG GGCTTTCTTC CGGAGCAGGG CAGCAGGCCC TTTCCTCTTC CTCGGAGAGC 600 CCAGCCTCTC CCCTCTCCCC AGCCCAAAAC CTCAGGGCTG GCGAGTGTGG GTGTCCCCGG 660 GCCGTGTGCG TCCCAACAGC TGCACTGCTT TCTGGCCCTG GAGCCTGTGG GTGTGACAAA 720 TGGTGTGGAA TGTGGTGGTC TCTGTCCTGT GGAGGTGGCC ATCAGGCCAG 770
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