Tag | Content |
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EnhancerAtlas ID | HS081-01718 | Organism | Homo sapiens | Tissue/cell | HACAT | Coordinate | chr1:206655640-206656910 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
HOXA13 | MA0650.2 | chr1:206655663-206655674 | CCCAATAAAAC | + | 6.62 | Klf1 | MA0493.1 | chr1:206656017-206656028 | TGGGTGTGGCT | - | 6.14 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | GTCCAGCTAG AGAGAGGTTG GACCCCAATA AAACAACCAG TAGAGAGCCA TTGTAGATTC 60 TTGACCTGGA AAGATGTGTT TGGGAAAGCT TTTTGGGTGT CTGTCTGCCC ACTTGCCCTG 120 GATGGACAGG CATGGTGGGG AATGGCACGC TGGCCTGGGT CTGGCGTCCT GGCATCCTGG 180 TGTCCGCTGG CTGCTGTTCC CCTGTTCTGG CTCTGCAGCC TCCTCCAAGG TGGCCTCCGT 240 GGTGTGTCTA GAGAGCTGGG GTCAGGCAAG TGCCTGCTTT GAAGCCTATT TCAGCCTCCC 300 ATCAAGGAGG AGGATGGTGA GCAAAAACAG TTGTGAGCAG GGAGCCAGAG GGCCAGGTGC 360 AGCCTCTTCT CTTAGTCTGG GTGTGGCTCC AGCCCATTGT CACCTTCCCC TACCTGGGCC 420 TCTGTGTCCT CATTTTCAAA ATGAGAGGGT TGCATGATCT CTGCGGCCTC CCAGCTCCCA 480 CATGTTGCAA GCCCATTCTT GCCTGAACAT CCCCAGACCT GTAGATTCTC CTAAGGGCTG 540 AAGACACTAG CTCCACCCGC AGTGGAACCA GGTATTTTCA TGAGCTGAAT GTCACACTGG 600 AGGAACCCAG CACCTCATGC CAAGTGGCCC ACCTTTGCCC ATCCTGGTGA CCCACCTCTC 660 CCCCAGTGTG CATATCCTGC CTCAGGTTCC CCAGGACAGG TCCTTTGGTA GAGCAACCTT 720 GCCTTTGTCC CAAAGCTCCC TGGCCCTCCT GGGCAGCTGC TGCCATCCAC AGGCACTGCT 780 CAGGCAGCCA GGACGGGCTT TGGGAATCCT AGGGCTTCCC CCAGCCCCGC CACCAGGCAA 840 GACATTCCAG GCAAGACTTC ATCTCCAAGG TCCCTTTTGA TCCCTATGAA TATCTTATTG 900 TGTCGCAGGA AGGAAATTTG TCTCCTCGTT TTATAGGTGA AGAGCCTGAG GCCTGGAGAG 960 CTAAAGGACT AACCCAAGGT CATGCAGATA GCAAATGCCA GGACTAGGAC TCGAACCCAT 1020 GTCTCCTGAC TCCCTGTGGA GATGTATTGG GTCCAGCCTC ACCCTCTTCT GCCGTCAAAT 1080 TTCCCATGCC TTAAAATCCA TTTGTGCACT CAGTAACGCC TTCAGCATCC GTGCACTGAC 1140 GGACTACCAT GTGCCGAACA CGTTGCTAGG CACGAGACGT ACGAGGAGCA AAGCGACGGC 1200 ACCCCTGTCT TCAAGGAGCC TGCAGTTCAT TCCTGATTCT CTCTTTGCTC AGCTCCCCTC 1260 TCCTTCCCTG 1270
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