Tag | Content |
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EnhancerAtlas ID | HS091-21889 | Organism | Homo sapiens | Tissue/cell | HepG2 | Coordinate | chr18:10546400-10547500 | Target genes | | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Sox6 | MA0515.1 | chr18:10546845-10546855 | CCATTGTTTT | + | 6.02 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | GGTATTCTTT GAAAGTGTTT GTTTTTGGTA TTACATTAGA TGATTTTTTA TACTGGTATG 60 AATAAGTACT TAAGAAAGGA TTCTATGGGT ATTTCTATGT TTTTGTAAAA TAATACTTCA 120 TGGGCCTCTA TTTTTGACCA AGATAGAGTA AGCCCACTAC AGCTTGTTTC TCTGCTGATT 180 ACAGCTAAAC TACTGGATAA AATACAAAAG CAACCACCCT TGAACTCTGA AAAGTAAATA 240 AAAAGAGACT AAGGAGAGGA GCAAACACGT GGAGAAACAA CCACCATGGG AATGAGTTTC 300 TCGGGTTTTT TTCCATTTCC TCTTGCAGCA TTCATTGCCC TGCCCTGAGA GAAGCCCACA 360 GTTGTGGAGC TGGGCAGCAA AGGCTGCAAC AATGAAAACT CCAAAAGAAA CCCCGCCTTT 420 CTAACCAGCA ATGGGAGAAG AGGTCCCATT GTTTTCCTCT CCTTTGGCTT TGCTCCAAGC 480 TTGTCCCAGG CATGGAGCTA CACTGTGATG ATGGCTCAGG TTGATAAAAC TCCACAAGGA 540 CCCCAGTCTC TTTTGCCAGA GGAACTAGGA AAATGAGCTA GAGAGCAAGG AGAAAATTCC 600 GGAAAGGAGA GAGCTGGAAA CGGAGTCCCC TGAGTGTGGA TGTGGCCCAC ACAAGTCTTG 660 GGTTTACTCT TCAGCTGTGC TGAGACAGGC CTCAAAGTAG CAGTGCAGCG CAAAGCTTGG 720 AGAGCTAAGA TTTCATCACT GTCGAAGTGT TGCACTGCCC TCTGAAGGGC TTATGCATGG 780 AACAGGCCCA AAGCCACATA GCAAAGGATT TGAATTAAGT GTAGAACTTC CATCCACCAA 840 AAACAAGGCA CCACATGTAG TCTGAACCTA ACTGGGGTGA TTACCTGCTG AAAACATCTG 900 TACTCTCCTG AAAATTAAGC AGAGGCTGTG CAGCATCACA TTCACAGTAC AATCCAGAAT 960 TACTCAACAT GCAAGAACCT GGAAATATGA CCAGTTTTCA GGAGAAAAGA CAACTGATGG 1020 CAACCCGGCA GTGACCAGGG TTGTTGGCAT TATCACATAA AGACTGAAGC AACTATAAGT 1080 TGCTCCATGA GGTAAAGATA 1100
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