Tag | Content |
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EnhancerAtlas ID | HS050-13134 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chr11:76504250-76505510 |
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) |
ZNF263 | MA0528.1 | chr11:76505039-76505060 | TCCTCCCCCTCTCTCACCTCC | - | 6.92 | ZNF263 | MA0528.1 | chr11:76505042-76505063 | TCCCCCTCTCTCACCTCCTTC | - | 7.26 |
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| Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
SE_00254 | chr11:76503160-76520678 | Adipose_Nuclei | SE_26826 | chr11:76503864-76505597 | Esophagus | SE_57060 | chr11:76503862-76504558 | VACO_400 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| Number: 1 | ID | Chromosome | Start | End |
GH11I076793 | chr11 | 76504060 | 76505493 |
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Enhancer Sequence | CAGATGCCTC TTTACATCGG CTGTTACTAC CATTGCCTCA GTTCTGTATC TTCTGGCTGC 60 TGGGTGATGA CTGCCCTGTG CCTGTGCACA GCCCTTCACA GTTGGCAGTA AGGGTTAATC 120 AACTTAGGTG AAGAGGGCAG GGCAGAAATT GCCACCCTGT AGTGCAGAGG ACAAGGCTGA 180 GGCTTAAAGA GGGGCAGCGA GAGGTCCCCT CTGGCGGGAT AGCATTTGGG TCGTATTTTG 240 AGCTGCTGGT TACATAAGTG GGAGCTCATA TGAGGCCATT TGGCATTTCA CGGACCCCTT 300 GTATAATCAC CTCTGGGAAT CAAAGGGTAA TCTCAGGGCC TTTGTGCTGT TTGTTTAAAC 360 CCCAGGAAGG GTGGGTATGA ATGAGCAGAT CAGCTTAGCA GGGGAGGTGG GGCCTTTGGT 420 GGTAATGAGC CCTGCGGTGA GGAGCTCGCC CAGGGGAACA AAAGGGGCCT GAAGCAACTT 480 AATATTTTCC TTTTGGTTCC AGACATTGGA ACACTCTGTC CTGCCTCAGC TGGGACCATG 540 CCCAGGATGC ACCTGGGCTG GATTTAATCC TGAAATTGGC CTCTACAAAA GAAAGGGGTG 600 GGAGAGGAGG GTCCCACATG GGGAGGGGGG CAGGGGAGAA GAGTCCCACT TTTCCCTGCC 660 CCTGGGCAAA GCCAGAGTGC AGATCAAGTG GCTAGCCCTT TAAAGTTTCA TGCAGGGCTG 720 GTAATGCAAT CCTGCTGCTC CCTCCCACCC ACCTTCCAGT CTGGAAGGTG GGCAGGTCCC 780 TGGCCCATCT CCTCCCCCTC TCTCACCTCC TTCCTGAAGT CCAGAGGGAG GGATGGGCAG 840 GAGGGCAGGG GCCCAGAGCA GGGCCACCCA GATGAAGAGC CTGGCTAGAA GGAAGCTTAG 900 TGCCTTCTGT CTCCCAGGCT GCTGAGGGGC CACTGTGCAG GGCCGGGGTG ACGACAGACT 960 ATCCAATTGG TCTAGTTAGA AGCTCCCACT GCCCAACCCT CTCCTTCTCA TGCTGGCACC 1020 ACTGAGCACC ACCATCCCAG GAGCTACAGT GGACGTGAAC ACAGGCTTTG AATCCAACAG 1080 CAGTGGGTGG TGTGACCATT AGATGTGACA ACACGTATGT AGCACCTGGC ATCTGTAGCA 1140 GCCACCACTG TAATTGTACA GAGGGAACTG AGATCTGAGG AGGGACACTG GCTCATGCCA 1200 CAGCATGTGT CAGTGGGAAA AGCCCCTCCT GCACCCTGCC TCTCCACCAG CTACTCTGCC 1260
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