Tag | Content |
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EnhancerAtlas ID | HS175-17527 |
Organism | Homo sapiens |
Tissue/cell | SK-N-MC |
Coordinate | chr20:56055500-56057260 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
POU2F2 | MA0507.1 | chr20:56056774-56056787 | ATTATTTGCATAT | + | 6.14 | ZNF263 | MA0528.1 | chr20:56056083-56056104 | GGGGGAGGAAGGGGCTGTGGA | + | 6.21 | ZNF263 | MA0528.1 | chr20:56057164-56057185 | AGGGGAGGAGAGGGGGAGGAG | + | 6.38 | ZNF263 | MA0528.1 | chr20:56057159-56057180 | GGAGAAGGGGAGGAGAGGGGG | + | 6.62 | ZNF263 | MA0528.1 | chr20:56057156-56057177 | GAAGGAGAAGGGGAGGAGAGG | + | 6.76 | ZNF263 | MA0528.1 | chr20:56057175-56057196 | GGGGGAGGAGAGGGGGAGGAG | + | 7.2 | ZNF263 | MA0528.1 | chr20:56057186-56057207 | GGGGGAGGAGAGGGGGAGGAG | + | 7.2 | ZNF263 | MA0528.1 | chr20:56057197-56057218 | GGGGGAGGAGAGGGGGAGGAG | + | 7.2 | ZNF263 | MA0528.1 | chr20:56057208-56057229 | GGGGGAGGAGAGGGGGAGGAG | + | 7.2 | ZNF263 | MA0528.1 | chr20:56057219-56057240 | GGGGGAGGAGAGGGGGAGGAG | + | 7.2 | ZNF263 | MA0528.1 | chr20:56057167-56057188 | GGAGGAGAGGGGGAGGAGAGG | + | 7 | ZNF263 | MA0528.1 | chr20:56057178-56057199 | GGAGGAGAGGGGGAGGAGAGG | + | 7 | ZNF263 | MA0528.1 | chr20:56057189-56057210 | GGAGGAGAGGGGGAGGAGAGG | + | 7 | ZNF263 | MA0528.1 | chr20:56057200-56057221 | GGAGGAGAGGGGGAGGAGAGG | + | 7 | ZNF263 | MA0528.1 | chr20:56057211-56057232 | GGAGGAGAGGGGGAGGAGAGG | + | 7 | ZNF263 | MA0528.1 | chr20:56057222-56057243 | GGAGGAGAGGGGGAGGAGAGG | + | 7 |
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| Number of super-enhancer constituents: 7 | ID | Coordinate | Tissue/cell |
SE_43635 | chr20:56046678-56058511 | MM1S | SE_54280 | chr20:56056009-56056835 | Spleen | SE_54690 | chr20:56055043-56057186 | Stomach_Smooth_Muscle | SE_58384 | chr20:55990107-56074254 | Ly1 | SE_59384 | chr20:56044028-56070796 | Ly3 | SE_59605 | chr20:56000010-56074239 | Ly4 | SE_67245 | chr20:56046678-56058511 | MM1S |
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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 |
GH20I057480 | chr20 | 56055358 | 56057418 |
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Enhancer Sequence | CAGGATCCCA ATCCCGAGGT GGTGTTCAAC CCCTGGGTGT AGGACCTCAG GTGAAGGGTT 60 ACTCAATTTG GGGCAGCTTC CCTAAGCCAT GATTGTGCCG CACGCATGGC TGGCAGCATG 120 GATGTCAGTG TGGGGAGGCC CAGGCCCTTG GAGGAGGCTG AGGCAGCCTT GTCTGGGACC 180 CCAGGTACGC CTCCAGCCAT CTTCCCCACA GCCCCTTCTC TGAGCGCGCA GCCATCACCC 240 CAGACCCGGG CTGATATTTT TAGCACACAG GCACCCTGCA CGGCCCTGTA CACTCTGACC 300 AAATTTAGAA ATCTCAAGAG ATCTTTGCTT TTCTACGCCT TCAGAAGGAG CAATGAATGA 360 AAAGGCTCCC AGCCTCCGGT TTAGTGAGAG CAAACCCTCC TGTTTGCAGG GCTCTCTCTG 420 GTAGGGAACC CCAAGCTTTA CTGTGCAGTG AAAAAAAGCC AGGTGCAGAA TCCTGTGTGT 480 GTTTTGGGTC TACGGTAGCA AATGCAAAGC AACCCCTGCA CCGTGCACGT GTGTCTGAGT 540 CAGCACAGCC AGCAGCGGGG CGTGGAAGGA GCCCCCCGCA AGTGGGGGAG GAAGGGGCTG 600 TGGAGGTGAT TACCTCACTC TCATGCAGGG CTGAATATTA CTGTTTCCCC TGTTAAACAA 660 GGGTGTATTA CTTCCGAAAT CTGACAACCC CAAGCACCAA AAGGTTTAAA AATATCTCGA 720 GATTGTAAAG CCTCCGACAG AATGCTGAAA CAGGATTGCA CAGTTGACCA GGAGCTTCTG 780 AGGTTGTGGC GGACCCTCCA TGTTTCTGAC TGCCGGACAG TCACAGCCCC CTCTTCCCTA 840 ATGCCACCAG ATGTTCCCTG GGACACCTGC CCCCAGCTCT AGTCCACATA ATGCTGCCCT 900 CCACCTCCAG ACCCAGGGGA GGGGAGTGGT CAGGGCCGGC CAAGCCAAGC ACCGTATGGC 960 CCCTGGTTCA GGACATCGCT GGGACCCAGA GGCCAGAGAC CTTCAGCTGG GATCCCCAAG 1020 GATCCCTTGG GACCCCTGGG ACTGTTGTCC ACCTCTGTGC CACCAGGAGA GGAGAGCCCC 1080 ACTAAGACTG GAGTGACACC GGAAGGTGCA ACCAAGAGCA GGCAGGGAGA ACACGGAGTG 1140 CAGGCGCTGC CTGAGCCCCT GCCCTGGGCT GTGTCGGGGG AGCTACTGTG GAACTTTCTG 1200 TCTATGCAGG CTCAGCAGGC CACAGTGTGC ACCACCCGGC TCCTGCCAGT GAACCTACAA 1260 ACGCTGATGG CTAGATTATT TGCATATGTG TTGTTAAATA TGGCCAATAT TAAAATTAAA 1320 TGATACAAAC ATGTAATTAA AGGAATTACA TTAAAAACAG AGATAATAGC TCCTCAGGAC 1380 ACCTCACTCC CTAATTAGCA TACTGCACTT CACCATTCCC CAGGCTCTTG GGGTGCCACC 1440 TCGGCTGCAT TTGGGGGAAG GAAATGCTTT AGGTCTGGAC GTGCATTCCT GTGCGTCCTC 1500 TGGATAGCAG GAAATCTGCC AGCATGGAAA TGGCAAATGC TACAAACAGG GGTCCCCCCA 1560 AAGCCATTGC TTCCCAGCAT GCCTCTGAGA GAAGCCCTGT AACACAGGCC AGGGGGCACC 1620 TGCTCTGCAG GACCCCAAGC AACAGGAAGG AAACAGGAAG GAGAAGGGGA GGAGAGGGGG 1680 AGGAGAGGGG GAGGAGAGGG GGAGGAGAGG GGGAGGAGAG GGGGAGGAGA GGGGGAGGAG 1740 AGGGCAAGGA GAGGTCTTCG 1760
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