Tag | Content |
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EnhancerAtlas ID | HS140-01863 |
Organism | Homo sapiens |
Tissue/cell | Namalwa |
Coordinate | chr20:56055390-56057260 |
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) |
FOXC1 | MA0032.2 | chr20:56055469-56055480 | TAAGTAAATAT | + | 6.14 | 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 | ATGGGTTTCC CGTGTACTGT AGCACTGTGA GATTTTATTT TAAAATAAAT GCATTTGATT 60 TTAAAAAGTG AGTTGGAAAT AAGTAAATAT CGGTGCGGGT GAATCCTAGA CAGGATCCCA 120 ATCCCGAGGT GGTGTTCAAC CCCTGGGTGT AGGACCTCAG GTGAAGGGTT ACTCAATTTG 180 GGGCAGCTTC CCTAAGCCAT GATTGTGCCG CACGCATGGC TGGCAGCATG GATGTCAGTG 240 TGGGGAGGCC CAGGCCCTTG GAGGAGGCTG AGGCAGCCTT GTCTGGGACC CCAGGTACGC 300 CTCCAGCCAT CTTCCCCACA GCCCCTTCTC TGAGCGCGCA GCCATCACCC CAGACCCGGG 360 CTGATATTTT TAGCACACAG GCACCCTGCA CGGCCCTGTA CACTCTGACC AAATTTAGAA 420 ATCTCAAGAG ATCTTTGCTT TTCTACGCCT TCAGAAGGAG CAATGAATGA AAAGGCTCCC 480 AGCCTCCGGT TTAGTGAGAG CAAACCCTCC TGTTTGCAGG GCTCTCTCTG GTAGGGAACC 540 CCAAGCTTTA CTGTGCAGTG AAAAAAAGCC AGGTGCAGAA TCCTGTGTGT GTTTTGGGTC 600 TACGGTAGCA AATGCAAAGC AACCCCTGCA CCGTGCACGT GTGTCTGAGT CAGCACAGCC 660 AGCAGCGGGG CGTGGAAGGA GCCCCCCGCA AGTGGGGGAG GAAGGGGCTG TGGAGGTGAT 720 TACCTCACTC TCATGCAGGG CTGAATATTA CTGTTTCCCC TGTTAAACAA GGGTGTATTA 780 CTTCCGAAAT CTGACAACCC CAAGCACCAA AAGGTTTAAA AATATCTCGA GATTGTAAAG 840 CCTCCGACAG AATGCTGAAA CAGGATTGCA CAGTTGACCA GGAGCTTCTG AGGTTGTGGC 900 GGACCCTCCA TGTTTCTGAC TGCCGGACAG TCACAGCCCC CTCTTCCCTA ATGCCACCAG 960 ATGTTCCCTG GGACACCTGC CCCCAGCTCT AGTCCACATA ATGCTGCCCT CCACCTCCAG 1020 ACCCAGGGGA GGGGAGTGGT CAGGGCCGGC CAAGCCAAGC ACCGTATGGC CCCTGGTTCA 1080 GGACATCGCT GGGACCCAGA GGCCAGAGAC CTTCAGCTGG GATCCCCAAG GATCCCTTGG 1140 GACCCCTGGG ACTGTTGTCC ACCTCTGTGC CACCAGGAGA GGAGAGCCCC ACTAAGACTG 1200 GAGTGACACC GGAAGGTGCA ACCAAGAGCA GGCAGGGAGA ACACGGAGTG CAGGCGCTGC 1260 CTGAGCCCCT GCCCTGGGCT GTGTCGGGGG AGCTACTGTG GAACTTTCTG TCTATGCAGG 1320 CTCAGCAGGC CACAGTGTGC ACCACCCGGC TCCTGCCAGT GAACCTACAA ACGCTGATGG 1380 CTAGATTATT TGCATATGTG TTGTTAAATA TGGCCAATAT TAAAATTAAA TGATACAAAC 1440 ATGTAATTAA AGGAATTACA TTAAAAACAG AGATAATAGC TCCTCAGGAC ACCTCACTCC 1500 CTAATTAGCA TACTGCACTT CACCATTCCC CAGGCTCTTG GGGTGCCACC TCGGCTGCAT 1560 TTGGGGGAAG GAAATGCTTT AGGTCTGGAC GTGCATTCCT GTGCGTCCTC TGGATAGCAG 1620 GAAATCTGCC AGCATGGAAA TGGCAAATGC TACAAACAGG GGTCCCCCCA AAGCCATTGC 1680 TTCCCAGCAT GCCTCTGAGA GAAGCCCTGT AACACAGGCC AGGGGGCACC TGCTCTGCAG 1740 GACCCCAAGC AACAGGAAGG AAACAGGAAG GAGAAGGGGA GGAGAGGGGG AGGAGAGGGG 1800 GAGGAGAGGG GGAGGAGAGG GGGAGGAGAG GGGGAGGAGA GGGGGAGGAG AGGGCAAGGA 1860 GAGGTCTTCG 1870
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