Tag | Content |
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EnhancerAtlas ID | HS147-00508 |
Organism | Homo sapiens |
Tissue/cell | NHEK |
Coordinate | chr1:16518100-16519010 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ZBTB18 | MA0698.1 | chr1:16518604-16518617 | ATTCCAGATGTGC | + | 6.03 | ZEB1 | MA0103.3 | chr1:16518467-16518478 | GGGCAGGTGGG | - | 6.14 | ZNF263 | MA0528.1 | chr1:16518320-16518341 | CCCCCAGCTTCCTCCTCCTTC | - | 7.05 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_26540 | chr1:16517842-16519062 | Esophagus |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr1 | 16518114 | 16518227 | chr1 | 16518530 | 16518700 |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I016191 | chr1 | 16517843 | 16519062 |
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Enhancer Sequence | AATCTTCTAA ACAATAGGCT CAGAGTTTGG GGACCAGGAG GAATGAGGAG GGGTAGCAGG 60 GTCCCTACAG TCTCTGCAGA GCAGGATCGC TGCAGAGAAG GGCATGGGCA CTGGGTGGGG 120 AGGAGCTCCT GAAGGACTGG AGACTGGCTG GGCAGACAGC CTCAGGGGCC AAAACTCCCA 180 CCCCAGACGC CATCTCCAGG TCCTGTCCTG CAGATACCAC CCCCCAGCTT CCTCCTCCTT 240 CTGCGGCAAG CAGGAGCAGG GCCCTGGGTC CTTGGCCAAA GCCCTACCAG GGCAGGGCAT 300 GATGGGCAGA GGCAGGCACC ACTGAGAGAG GGGCTCCCCT GAGATGCCTG GCCCAGATCT 360 ACCCCCTGGG CAGGTGGGCA GGGAGCAGGT GAGGAATGAG GGAAGTGGGC CAGGTGAGCA 420 GCCCTGGCCT CCTTGCCTGA AGCACAGCCC CAAAGCCAGC CCCCTGGCCC CCAGCAGTCT 480 AACCCAGACT CAGGTGTCAG CCAGATTCCA GATGTGCCAG GGCAGGCTGA ATGCAGGAGA 540 GCCTGTTTCC TCTGCTCTGC CAAGCTGCTG CCAAGTTGGG CGCTCTTCAG GCAGACTCAG 600 CACTGGAAGA AACACACAGG CCCCTTGGTC TCTACTCAGT ACAGGAATCC CATTCCCAGA 660 CTGCCTGAGT TCCTTCAATC CTCAGGGGAC GGGGGCCTCC CCACCTCGCA AGGGCCCCCA 720 TGCTCTGGCT GTGCAGCTCT GACACAATAA AAGCCACCAC TTCTCTTGAC TAATTATGGG 780 CCAGACACTG TGTCAACCAC TTACATACTT CATTTCATGG TGGCTCCATG AGGCAGGAAA 840 CGTTATCACC GTCCCCATTT TGCAGATGGG GCTTGGAGCC TTAAAGAGGC TGTAAAGAGA 900 GTTGGTGTCT 910
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