Tag | Content |
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EnhancerAtlas ID | HS150-01429 | Organism | Homo sapiens | Tissue/cell | NT2-D1 | Coordinate | chr1:226683930-226685200 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr1:226684662-226684680 | GGAAGAAGGGAGGGCAGG | + | 6.29 | EWSR1-FLI1 | MA0149.1 | chr1:226684653-226684671 | GGATGGAAGGGAAGAAGG | + | 6.67 | EWSR1-FLI1 | MA0149.1 | chr1:226684657-226684675 | GGAAGGGAAGAAGGGAGG | + | 6.68 | Nkx2-5(var.2) | MA0503.1 | chr1:226684274-226684285 | AAGCACTCAAG | + | 6.02 | ZEB1 | MA0103.3 | chr1:226684924-226684935 | GGGCAGGTGGG | - | 6.14 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | TGTTTGCACT TATAAACCCA ATGCTATGAA TAGGAATGGT GAAGAGAAGA GTCCTCACGC 60 TTTTGAAATG GAGATAATTG ATTGATTTTC TAATATTGAT CATTTGCAAA ACAATACGCA 120 TATATACTGC CCGAGACCGA TGCCACAAGT CAACATGATA GTCGGCCACA TCGCTTTAGA 180 GACACCCCTC ATCCTGCCCA GTACTGTTCC CTGTACCTGC ACATTTGCCG TGCCCTTGGT 240 GTGACGCACC TGCAGGAAGG CGAGCAAGAC AGTGCAGATG CACAGAGCCC ATATGTTTCT 300 CACATTAGCA ACACAAAGAG GTGAGGCTGC ATTTCCTACT TGTCAAGCAC TCAAGCTTAA 360 TTGGGCCAGA AATACTCTCT GGTTCCTGCT TCTGCAAGAC AGATCTTGGC TGTCACTAAG 420 CATCTGTGGT ACCCGGAAGG GACAAATGGA GTTCTGTGGG CTGGAGGCTT TGAGAAAGAG 480 CAGATTTTTT CCTCCATGCC AATTATGTGT GTGGGATTTG GTTTTCTTTG TGTGTCCCAA 540 CCTTTGGCCC CAGGGCTGAC ATTCTGAGCA TGCCTGTGTC CCCGGCACTC TGCTCCCACC 600 ACGATGCACA GGAGGCCAGC TGAATCCCTG GCACTGCAGG TGTCAGAGCA AGAGTGTTCC 660 AAGCAGGGAG GCGGGGAAGC TTCCAGAGGC AAGGGAGGTG GAACCTGAAG GGGTGAAGAG 720 CATGGATGGA AGGGAAGAAG GGAGGGCAGG CAGGGGAGCT GTGGGAGCAA AGACAGGGTG 780 GTAGCACACT AGTGCATTCA CTTGTTCAAT AGTATTTATT GAGCACTTAC TGTGTGCAGC 840 AGCGATCAAG GCAGACCCTG TTCCTGCTGT CAGGGAGAGA GAGGCAGACA ACAAGCAAAT 900 GACCAGGTTT GATAATATCT GCAGTGAAAT GTGCTCTGAA GAGAAACGGT GCAAGGTAAA 960 GGGTAAGGAA GGGAACAGGG GGTTGGTTTG GATGGGGCAG GTGGGGCAGA GTGAACCAGA 1020 CCAGCAGGGC ATTTGGAGGA CCAGGCAAGG GAGTGGTTGG CGAGATGCGG GCTTGGGGAC 1080 CTTGATGTAG GCTAAAGAGT TTTGGTGGAA CCTGATGGGC AGTCATCCTT GATGGTACCC 1140 ACAGGAGTGG GGAGGGGAAC TGCTAGATGT TTGGGCTAAG CCCTCTGCTC TGTGAAGGAA 1200 TTCATTACCT TCTCCACGCA AATCCTTCAA GCCAGTGCGG AGGTGTCAGT ATGTGGGAGC 1260 AACCAGTGAT 1270
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