Tag | Content |
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EnhancerAtlas ID | HS048-27415 | Organism | Homo sapiens | Tissue/cell | Fetal_small_intestine | Coordinate | chr4:18021790-18023220 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
RFX1 | MA0509.2 | chr4:18022472-18022488 | CGTTGCCGTGGCAACA | - | 6.35 | RFX1 | MA0509.2 | chr4:18022472-18022488 | CGTTGCCGTGGCAACA | + | 6.36 | RFX2 | MA0600.2 | chr4:18022472-18022488 | CGTTGCCGTGGCAACA | + | 6.36 | RFX2 | MA0600.2 | chr4:18022472-18022488 | CGTTGCCGTGGCAACA | - | 6.3 | RFX5 | MA0510.2 | chr4:18022472-18022488 | CGTTGCCGTGGCAACA | - | 6.75 | RFX5 | MA0510.2 | chr4:18022472-18022488 | CGTTGCCGTGGCAACA | + | 6.87 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | CTGAACTGAA ATTGTATTAA GTTTAACCTA ATACGATCTC TTCTCTACTA GTCAAAAAAA 60 GATCTTAAGA CGTTAACCAA ATACATGGGA GGCGGGGTCG GGGGTGCGAG GTGGTGCCAG 120 AGCAGATGGA AACAAGGTAA GAGAGTTGTT TTCTTAAGAC ACTAGGGTTA CTCCCCAACT 180 CCAAATGCCA AGATTCACTC GCCAGTAGAG CAAGCTGCTG CCACTATCCA CTGCTTACAC 240 AATACAACCT TCCTTTCTAC CTCTTCCCCT ACACTCCCAC CCATAACCCC CTTCCAAAAC 300 AAACACCCAC AACGCGCCCC ATTCCATAAT CCGTGTTCGC CCCTCTAAGC CCACTAAACC 360 AACCTGCTGG ATAACAGCTC TATGCATTCG TCTTAGGCAA AAAAAGAAAA AAAAAAAAGC 420 GACTGCAGCA AGGTCGGGAG TCCCACCATT CCTGTCACCC TAAACAATCC ACAGGGTGAG 480 AGCCCCAAGC CCAGAAGTTT GAGGCAAAAC GATTCAGATC CAACCAAAAA GAGGGAATTG 540 CAGTTGAATG GGGATGGGAG GTGGGGAGGG CGATGCGTAT GCGTGTATAT GTGTGTGTGT 600 GTGTAAGGAA GAGTCCATCA CATGACAGTG AAAGAGGACC AGAGTCGTCG GGGCGTCCGC 660 AAGCAGACGG GGGGGAGGGT GTCGTTGCCG TGGCAACACC CCCCATCCGT CCAGACTTCC 720 AAAGAGGGAG GAAGAACTTC AAATCCCAAC CGTCAGCGCT CAAGCGGCTC CTTCTTAAAG 780 GGGTACACAC AGCGCCGCCG CCGAGCGCGA GAGGGCAGAG TTGGGCGCCC CCCGCCCCTC 840 GGACGACGCC CCCGCCGCCC CTCGCCCCCA GCCGGCCCAT CAGCGGCCCC CGCCCTGCGA 900 GTGCCCGTGG GTCTCCAGGT CCAGGTCCCC GGGAACTGGC CGCGTCTGCT CACCCGGCCC 960 CCGGCGGCGA CAAGGGGGTG TGTGTGCGCT CGGCGGGGGC GCGGACCAGC CCGCCTTCCT 1020 CCGGCCGCCC TGCCCGCCGG CTCTCCTCCG CCAGGGCGCC GACCCACCGG GCCGCTTCCT 1080 CCGTCCTGTC AGGGTGGACG GCGGGCGACG GCGGGCAGCG ACGGGCGCCG AGGAGTTTCG 1140 GGGAGAGAGC GAGCGGGCGG CTTCCGCGGG GGCTCAGCAA GCGGGTCCAA ACTAACAGTT 1200 CCCGGGGAGC CCAAGAGCTG GGAAGGCGAA GGAGCGCGGA CCGCGCCGGG CCAGCAGCCC 1260 GCAAGACAAA AGGCGAGCGC CGGGGCCGCC GCGCCGCGCC GCTCCCATCT CGCTCCCCCA 1320 CCGAACTAAC CCGAACGGGA GATTCAACTA AACCCCTCAG CCACAAACTC CTCGGGCTGC 1380 GACAGCGGTC GCCGCGCGGA GCCCGGGGCC CCGGCCCGCG TCTCTCTTAC 1430
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