Tag | Content |
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EnhancerAtlas ID | HS147-31499 |
Organism | Homo sapiens |
Tissue/cell | NHEK |
Coordinate | chr4:100636020-100636980 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
HNF1A | MA0046.2 | chr4:100636538-100636553 | TGTCAATTATTAATC | - | 6.17 | HNF1B | MA0153.2 | chr4:100636539-100636552 | GTCAATTATTAAT | + | 6.08 | MEF2C | MA0497.1 | chr4:100636733-100636748 | TTCTATTTTTATATA | - | 6.36 | POU2F2 | MA0507.1 | chr4:100636762-100636775 | TCCATTTGCATAT | + | 6.23 |
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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 |
GH04I099714 | chr4 | 100635978 | 100638872 |
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Enhancer Sequence | TGCTTCCTAC CCTAGCCTCC TGTCCACAAA ACTATCTTTG AAAAATTTCT AACCTCTGAG 60 CCTTCAGGGA TTCATTTGAG TAATAACTCA GTCTCCCACA TGGCATTGCT GGCCTTATGT 120 CAATTAAACT CTTTCTTTAC TGCAATGCCA TGGTCTTGGT GAGTTGATTT TATTTGTGTA 180 GTGAGCAGGA AGAACCCATC GGGCAGTTAC GGGAGTGTGG AAATAAACAA AGACCAACCA 240 AATGAGAAAA GCAAAGGTTA TTTATTCTGA GCTTGCTATA GCAGAAGAGT CTGCATCATC 300 CCTTGAGTTT TGGCAGAGAT TTAAAGGCAG GCAAAGAAGT GGGAAAGCTT TACAATGGAA 360 AAAAGGGAAG GCTTCAGGCA TGCACTGATC GGAGGCTTTG GCCTGGGGAA GCTATAAGTG 420 GGCTAACCAG AATCAGGTTG TCCTGTGTGA TTAGTTAGGG GTATATATTC TGATTTCTCT 480 GGTCCTAGGT TGGAAGCAGA GATCAAAATT AGGGATGCTG TCAATTATTA ATCAAGTCCT 540 GGCTATTTGG GGCCTATTGC TATAGCAGCT ACTGTTTAGC TTCCTGGATC ATCACTACAG 600 ATAGCAATCT GGCTTCCTGC AGGTCTGACT TACAGCAGGA TGGCTTCTTG TGTTGCTCAT 660 TGCAGATAAG GAGCTGGTTT CCTGGGCAGG TTTCTACAAG TTGTGGATCA AAGTTCTATT 720 TTTATATATG GTCTGGACAT TGTCCATTTG CATATCAGTC TCTTGGGAGT CTCTATTGTT 780 TGTATTCAAA TTGATCACCT AGTCCTTCAT AGGCCTGGCT CTCTGATCAC TAAGATGGTT 840 TCTTTCCTTT TCTGCTTCTA AAACCATTTC TGTTTCTAAA CTAAGACTAT CTCAGCTTTA 900 GAAACTCTCA TACTGCAGGA AAGTCTTCAG TTCCAGGCAA ACTGGGATGG TTAGTTATCC 960
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