Tag | Content |
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EnhancerAtlas ID | HS101-01989 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr1:86894950-86896390 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
RUNX1 | MA0002.2 | chr1:86894955-86894966 | CTCTGTGGTTT | + | 6.14 | ZNF263 | MA0528.1 | chr1:86896028-86896049 | TTTTTTGCTCCTTCCTCCTTC | - | 6.16 |
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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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| Number: 1 | ID | Chromosome | Start | End |
GH01I086428 | chr1 | 86894502 | 86896754 |
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Enhancer Sequence | AGCCGCTCTG TGGTTTCCTT TTCAAATGTT ATCGTACTTA ATTCTAGCAA CTCTAAGCGA 60 TGAGAAATAC TCCAGAGATA AAAAACAAAA AGAGGTCTGA ACTGCTGCAG AAGGAAAGGC 120 AAGAGGCACG TGGAGACAGC ATTAAGGAAC AAGGCACACA CCAGGTTTTT GTCAGACATG 180 GAAAAAACCA GCTTCAAGAA GAAATCCCAC AAGTCTGGAT CTAGGCAAAT TCATTGTGAA 240 GAGCAATAGA CTATGCCAGG GAAAGTGGTT CAGCCTGTGG TTAGATATTG ATGGCTGGAG 300 TTTGGGAGAG AAGTCAGGGT CATAGGCCTA GAGACTGGTA TTTAGTGAGT GAGATCTGAG 360 GGAGAAAATA GTAAGCACAG TTCGCCAGTC AAGGACTATC TATCCCAATC TTTATTTTTT 420 GTTTTTGATT TAATGTAACA GTAGTGCCTT TCAAGTGATG TCTTAATTTT CTTTTTTATC 480 CCTAGTTAAA TCTAAACTAG GGTTTTGTTA ACAAGGATTT TGTTATCCTC TGTATAGTTA 540 GCAGGAAGTG GAGTGAAACA CTCCATAAAA TACACTTTAC AAAACACTTT ATAAATCTTT 600 AGAAAAACGT AGTTTTTTTT CTTTCCTGGT AACCTTGAGA TGCTGATAAT CTCTGCTCAA 660 GCATGATTTC ATCAGCACTT CTAAATTTCA TGAGTAGGCA CAATCTTTCC CTCAACACTC 720 ACAGCTTGGA CTGCTACCCT CCCTTCCTTT GCCTCGAGGT CCAAAAATTA CACAATATGC 780 CACAGCCTGA GTCAACTCAG CACACACTTC CTGAGTTCCC GGAACTTAAA ATAATTCAGA 840 AAAAAGAAAT GTGTGCTTTG GGAGGGGAGT TCATCTGGAA AGCTTATATG GGAAAGCTGT 900 GGTCTGAACT TTGAAGGGAA TGTAAGATTT TGAGAGAGAG GAAGTTCTAA AGGATCTCAT 960 GCAGAGGATG GGGGTTTCCC TGACCTAGGA GCTGTAAAAT ACACATAAAC ATGGAGAATA 1020 AGGGATAAAA TAAAAGAGAA GGGACCATCC AGGCTGGGGA GAACATTCTG CAGTCTCCTT 1080 TTTTGCTCCT TCCTCCTTCC CTAGCTCCTA GGTTTCAACT ATTGCTCTAG ATAGAAGAAT 1140 TACCTGCAAG AAAAAAAGCA GGTCTGCTTG GATAGCTCAG ACAGAAGATT AGGAAAGCTT 1200 TATTTGCCTA TCTGGATATG CTTCTTTCCC TTTCTCCAAA CCCTGAACTT AGAGGCCTCT 1260 ACAAAGCTGA ATAGAAACCT GTTGGGCAGC TTCACTGGGG AGATGAGAGG ATGTGGGACT 1320 ACTCACTAGC TTCAAATAGA TGTGCAACAA GTAAATTACT GCATTTACAA GACCAAACAT 1380 ATTTTCATGC TGCCTTTTTT ATGGTGGTAG GTGGTGGAGT AGGAGGAGAT GGGAATAGGA 1440
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