Tag | Content |
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EnhancerAtlas ID | HS034-05683 |
Organism | Homo sapiens |
Tissue/cell | ECC-1 |
Coordinate | chr11:76504230-76505440 |
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 | TAACTCCTGC CCCTTTACAT CAGATGCCTC TTTACATCGG CTGTTACTAC CATTGCCTCA 60 GTTCTGTATC TTCTGGCTGC TGGGTGATGA CTGCCCTGTG CCTGTGCACA GCCCTTCACA 120 GTTGGCAGTA AGGGTTAATC AACTTAGGTG AAGAGGGCAG GGCAGAAATT GCCACCCTGT 180 AGTGCAGAGG ACAAGGCTGA GGCTTAAAGA GGGGCAGCGA GAGGTCCCCT CTGGCGGGAT 240 AGCATTTGGG TCGTATTTTG AGCTGCTGGT TACATAAGTG GGAGCTCATA TGAGGCCATT 300 TGGCATTTCA CGGACCCCTT GTATAATCAC CTCTGGGAAT CAAAGGGTAA TCTCAGGGCC 360 TTTGTGCTGT TTGTTTAAAC CCCAGGAAGG GTGGGTATGA ATGAGCAGAT CAGCTTAGCA 420 GGGGAGGTGG GGCCTTTGGT GGTAATGAGC CCTGCGGTGA GGAGCTCGCC CAGGGGAACA 480 AAAGGGGCCT GAAGCAACTT AATATTTTCC TTTTGGTTCC AGACATTGGA ACACTCTGTC 540 CTGCCTCAGC TGGGACCATG CCCAGGATGC ACCTGGGCTG GATTTAATCC TGAAATTGGC 600 CTCTACAAAA GAAAGGGGTG GGAGAGGAGG GTCCCACATG GGGAGGGGGG CAGGGGAGAA 660 GAGTCCCACT TTTCCCTGCC CCTGGGCAAA GCCAGAGTGC AGATCAAGTG GCTAGCCCTT 720 TAAAGTTTCA TGCAGGGCTG GTAATGCAAT CCTGCTGCTC CCTCCCACCC ACCTTCCAGT 780 CTGGAAGGTG GGCAGGTCCC TGGCCCATCT CCTCCCCCTC TCTCACCTCC TTCCTGAAGT 840 CCAGAGGGAG GGATGGGCAG GAGGGCAGGG GCCCAGAGCA GGGCCACCCA GATGAAGAGC 900 CTGGCTAGAA GGAAGCTTAG TGCCTTCTGT CTCCCAGGCT GCTGAGGGGC CACTGTGCAG 960 GGCCGGGGTG ACGACAGACT ATCCAATTGG TCTAGTTAGA AGCTCCCACT GCCCAACCCT 1020 CTCCTTCTCA TGCTGGCACC ACTGAGCACC ACCATCCCAG GAGCTACAGT GGACGTGAAC 1080 ACAGGCTTTG AATCCAACAG CAGTGGGTGG TGTGACCATT AGATGTGACA ACACGTATGT 1140 AGCACCTGGC ATCTGTAGCA GCCACCACTG TAATTGTACA GAGGGAACTG AGATCTGAGG 1200 AGGGACACTG 1210
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