Tag | Content |
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EnhancerAtlas ID | HS095-08399 | Organism | Homo sapiens | Tissue/cell | HMEC | Coordinate | chr13:45165320-45166540 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Znf423 | MA0116.1 | chr13:45165404-45165419 | GCCACCCTGGGGGCC | - | 7.52 |
| | 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 |
GH13I044591 | chr13 | 45165641 | 45165790 |
| Enhancer Sequence | TACAGGGAGG AGGCAGACTG CCCCCACCCC TCTACCCCCA ATTCCTCCAC CCTTCCACCC 60 CACCGCAACC CCCAGCCCCA GCCCGCCACC CTGGGGGCCG CCACAATGGG GCCTGGCCAA 120 GTCGCCCGCC TGGCGAGGGG GAGCTCCAGG CCACCCCTAA GAGCCAGGAC CACAGCAGGA 180 GCTTTCAGCA ATATCGCCCC TACCCGAGAT GCCGGTCCAG ACCCAGTGAG GACCTGGAGC 240 CCCTGCCCCA GGCTTCGAGG GGGCGCTGCC GGTTGCCGGT GCGAGGCGCT GGGAGCCAGG 300 GACAAGCGGG AACTCTGCTC CTTACAAGTT AGTGGGGCGG GACCTCCCCA GGTACAACTG 360 CAGCTGCCTA AGCTACAGCA GCAACTCCAG CACCTCTGTG CTCTTGGGAG CCGGGAGTAG 420 GCAGGAGCTC CGCCCTCCTG GGCGGGGCTA CAGCCTCCCA AGTCTTGGCT GTGGATCAGG 480 GCCTCCAGCT CCCTGCAACA GGCAGGAGCC CCACCCCACC CCACTGAAAA CCGGGGCTGC 540 AGCGCCAGGT ATCCTGCAGG CCTGGGGGGC CTGGGAAGGC CCCCCCATGC CCTTGCAGAC 600 TCAGAGGTGC CTACTCCCAC TGTCTAGCAT CTCCCCACTC CCAGGGCCTA CTCTGATCTT 660 AAAGTGGGAT TTGGGTGGAG CCCAAGCACT GTCACAGCCA GACCAGGTAT GCGTAGGCTT 720 GGGCCAGTGC TGACATGCTA TCCCTCTGCC ACCTCGGCCC CCTCTGGATT TTGGGCACTG 780 AGGAGCACAG GAGGGGAAGC TGAGGGTGGC TGGGTAGTGG CCTGCAGGTG CCCTTTGATG 840 CCAGCACCCT GCCATGGATG GCCGCAGGAG GCAGACAGGC TCCTGGGCAG AAGGGCGCTG 900 GTTCCTAGCA AGGCCCACCT TCAGGCCAGG GAGGGCCTAA AGGCTGAGCA CTGGGCTACC 960 AGTTCATGAA TTGGAATGAG GACTTGTGGT GCCTTCTCTG GGCTGCCCAT GGCCGCCCAT 1020 GGACCAATCG GCTGGCACTT CTTCCCCTCT AAGGTCCATA AAAGGCTCGG GCTCAGCCAG 1080 AGCAGGGCAG AGGGCAGAAG ATGGAGAGAT AACAGGAGGA CCAGCTGCAA AGAGGAGCTA 1140 CCCTCTCTGC TGAGCACTTC AGAGGCCTGC AGAGATGTCT GCACAGCCTG TGGAGAGGAG 1200 CCACCCTTTC CAGGGCCTCC 1220
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