Tag | Content |
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EnhancerAtlas ID | HS108-17009 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chr17:42955440-42956920 |
Target genes | Number: 16 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CTCF | MA0139.1 | chr17:42956178-42956197 | TGGCTCCCTCTGCTGGCTG | - | 6.82 |
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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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Enhancer Sequence | TTGCAGTAAA CTGAGATCGC ACCACTTCAC TCCAGCCTGG GCAACAGAGC AAGACTCCAT 60 CTCAAAACCA AAACAAAACA GAAGGAATAA GAAGAGTTAG AAGACTCACT ATTTGCAACT 120 ATTGTAGGAA CAAGCCAAGA ATCATCAATA GATGACAAAA CTAGTAGATA AAGTTTGATA 180 AGGAGAAGAA TAACCAGATT CTAATAACCA GAGCTTAATC ACGAGGAAGT ATTAGACAAA 240 CCCAAATTGA AAGACATTCT ACAAAATAAG TGCCCTGTAC TCTTCAAAAG TGTCAATGTC 300 ATAAAAGACC AAGAGAGGCT AAAGAACAGC TTCAATTCAG AGAGACTTGA AAATCATGAA 360 AACTAAATGT TATGCATCAC TCTGGATTAG GGGAAAAAAT TCTATAACGG AAATTGTTGG 420 TATGATTAAT AAAACTGAAT AAGGTCTGCA AAAAAAGATC TGTACAACAG GACTGTATCA 480 ATGTCAAATT TTCTGATTTT GGCAACTGTA CTGTGGTTAC ATAGGTGAAT GTCCTTATTC 540 TTAGAAAATA CATTCTGAAA TATTTTACTT TCAAACAGTT CAAGGGGAAA ATGTACACAC 600 CTGTCTCTCT GTGTGTGTCT GAACGTGTAC AGAGAGAGAA TTACGAAGTA AATGAGGGTG 660 GGTTCTTTGA ACAATTCTTG AAGCTTTTCA GTTTGCTGCT ATTCCAAAAT GAAAAGTCAG 720 TTTAAAAAAA GACAATTCTG GCTCCCTCTG CTGGCTGTCT CACCAATGAT AACACGAATA 780 AGGTTAGCCA AAGTGTTCCA TCTCTCAATT GAGGAATACA GAAGACACCC TGGTATTTTA 840 ACTCCAATCT CTTGGAAAAA CACAACTAAT ATTAAAAATC CACTTACAAG AACATACACT 900 CCTCCCTTCC TTTTATTTAC ATTTGTCATT TTATCTTTGT GTTTTCTGAA TAGCAATGAG 960 TCTTATCATT TTGAGCTTCA CTGAGCAGGA AGCAAGGGCA CCCACATTGA TAATTTTTTT 1020 CTTCGTTTTT TGAGAGAATG TCTCACTCTA GCACCCAGGC TGGAGTGAAG TGGCGCAATC 1080 TCGGCTCACT GCAACCTCCA ACTCCCAGGC TCAAGTGATT CTCCTGTTTC AGCCTAATGA 1140 GTAGCTGGGA TTACAGGCAT GGGTCACCAC ACCTGGCTAA TTTTTGTATT TTTGGTAGAG 1200 ACGGGGTTTC GCCACGTTGG CCAGGCTGGT CTCGAACTCC TGACCTCAGG TGATCCACCC 1260 ACCTCAGCCT CCCAAAGTGC TGGGATTACA GGTGTGAGCA ACCACACCCG GTAAGAATTA 1320 ATTTTGAAAC ATTTGCTGCT TTAATTTTAG AGCAAATTTG AGCCTTAATC CCAGAGAGTT 1380 TCAAGTTCTC TGGCTCCCAG CTCACTCAGT GCTCTGGGTA TTGTTGCGGG GTGGGGGCAA 1440 ACATAACAGG TGGATGAGAT TCTGGGAGCT GAGTCTGACT 1480
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