Tag | Content |
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EnhancerAtlas ID | HS110-05007 |
Organism | Homo sapiens |
Tissue/cell | KATO3 |
Coordinate | chr9:104242210-104243640 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Foxd3 | MA0041.1 | chr9:104242647-104242659 | GTTTGTTTGTTT | + | 6.32 | Foxd3 | MA0041.1 | chr9:104242651-104242663 | GTTTGTTTGTTT | + | 6.32 | Foxd3 | MA0041.1 | chr9:104242655-104242667 | GTTTGTTTGTTT | + | 6.32 | Foxd3 | MA0041.1 | chr9:104243465-104243477 | AAACAAACAAAC | - | 6.32 | Sox6 | MA0515.1 | chr9:104242265-104242275 | AAAACAATGG | - | 6.02 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr9 | 104242724 | 104243083 | chr9 | 104243394 | 104243447 |
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| Number: 1 | ID | Chromosome | Start | End |
GH09I101478 | chr9 | 104240578 | 104244329 |
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Enhancer Sequence | TTTACATCCT TGTTTCAGTG TGCCACAAAT CAAGTCCACT CATCATTCAT TGGCCAAAAC 60 AATGGGACAG GAAGATTTAC TCCTCCCACA GAGCAGAAGG AGGGGAAAAT GAAGATTCAA 120 TAGAAAAAAA AAAGGCAACA GGCCAATTTC TAAATCCTCA GGAGAAAAGA AAGCATCTAG 180 CAATCTGCTC ACGGAGTATG GAAATTTTTT TTAGAATGCT TACAGGGCTT AAGACCCGGC 240 CCCCAACCCC AATCATTACA CACTACACGA ATAAGGACAG GCTTCAGTAA TGATCCCCAA 300 AATCTCAGTG GCTTATAAGA ACTAAGGTTT AATTCTTGTT CATAGTACTT GTCCTTTACA 360 GGTCAATTGT GCCTCTGTTG CCTGTTGTTT GTACTCTAGG ACCCAGGCAG ATAGAACTGT 420 TTTTTGTTGT TGTTGTTGTT TGTTTGTTTG TTTGTTTTTA ACATTGCTGG TTTTGTGGTA 480 GAGAGAAAAA AGGGGAATAG TGCACCACAA GCTGGCTCTC AAAGCCACTG CTCAAAAGTG 540 ACACAGATCA CTTCCACCCA CATTTCACTG ACTGGAACAA ATCACATAAT AACTCAAATT 600 CAACAGAGCA GAAGGGAGTG CCAAAAGATA CATGGCCACA CCTGAGACCA ATGACTGGAG 660 AAATATTTGT ATTCCAGGGA GGGGCAGAAA ATGTACTCCA GGGAGGGGCA TTTTGAACAT 720 TAATGCAATC TACCACACCC ACCTAGGACA CAGGAGCTGG GATCAGATCC TTCATTCAAG 780 ATTAGATGAC TGCTTTGCTG AAAATCCAAC CACATGGAGT TATGTAGTCA TTCAGGAGTA 840 TGTTCTTGTT TACTTTTTAA AACATTTTTT TAAAAGATTT AACCAATTGT TGCACAGTAG 900 CCTGTGGTGT CCAATGGCAC CTATAATTTA TTTCACCTTA CTGATCTGGT TTTAAGAAGA 960 ATGGCCAGCT GGATGTGGTG CCTGAAGCCT GTAATCCCAG CACTTTAGGA GGCTGAGGCA 1020 GGTGGATGGC TTGAGCCCAG GAGATTGAGA CCAGCCTGGG CAACATGGCA AAACCTAGTC 1080 TCAACAAAAG ATACAAAAAT TAGCCAGGCA TGGTAGCATG TTCCTGTAGT CCTAGCTACT 1140 CAGTAGGCTG AGGCAGGAGG ATTGCCTGAG CCCCAGCAGG TCGAGGCCGC AGTGAGCTGT 1200 GATCGCACCA CCGCACTCCA GCCTGGTTGA CAGAGAAAAA CCCTGTCTCA AACAAAAACA 1260 AACAAACACA CAAACAAAAA AAGATAAAAG ATAAATGGCC TTAGGGGAAC AGATATAAAA 1320 ACATAGGATT TTTCACTGCT AGTTTGGGGA AGGAGTTTTT TTACTCCCAG CCCAATCATA 1380 AGGGTGAGAC AAGAGGGCTA TGTCTATGTT ACCACTCTGA TTGTCTTTTT 1430
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