Tag | Content |
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EnhancerAtlas ID | HS089-09648 | Organism | Homo sapiens | Tissue/cell | Hela | Coordinate | chr4:18021660-18022580 | 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 | ACCAAAATAC ATTTTTCGTA AGGGCAAAAC AAAAGCAGTA AATTACTTAA ACATCACTTA 60 AATGCCCCCT AAAGTAACCT TCCTTTCTCA TACATTTTCC TATATTCATC GCGTTCTGCG 120 GTACACATTT CTGAACTGAA ATTGTATTAA GTTTAACCTA ATACGATCTC TTCTCTACTA 180 GTCAAAAAAA GATCTTAAGA CGTTAACCAA ATACATGGGA GGCGGGGTCG GGGGTGCGAG 240 GTGGTGCCAG AGCAGATGGA AACAAGGTAA GAGAGTTGTT TTCTTAAGAC ACTAGGGTTA 300 CTCCCCAACT CCAAATGCCA AGATTCACTC GCCAGTAGAG CAAGCTGCTG CCACTATCCA 360 CTGCTTACAC AATACAACCT TCCTTTCTAC CTCTTCCCCT ACACTCCCAC CCATAACCCC 420 CTTCCAAAAC AAACACCCAC AACGCGCCCC ATTCCATAAT CCGTGTTCGC CCCTCTAAGC 480 CCACTAAACC AACCTGCTGG ATAACAGCTC TATGCATTCG TCTTAGGCAA AAAAAGAAAA 540 AAAAAAAAGC GACTGCAGCA AGGTCGGGAG TCCCACCATT CCTGTCACCC TAAACAATCC 600 ACAGGGTGAG AGCCCCAAGC CCAGAAGTTT GAGGCAAAAC GATTCAGATC CAACCAAAAA 660 GAGGGAATTG CAGTTGAATG GGGATGGGAG GTGGGGAGGG CGATGCGTAT GCGTGTATAT 720 GTGTGTGTGT GTGTAAGGAA GAGTCCATCA CATGACAGTG AAAGAGGACC AGAGTCGTCG 780 GGGCGTCCGC AAGCAGACGG GGGGGAGGGT GTCGTTGCCG TGGCAACACC CCCCATCCGT 840 CCAGACTTCC AAAGAGGGAG GAAGAACTTC AAATCCCAAC CGTCAGCGCT CAAGCGGCTC 900 CTTCTTAAAG GGGTACACAC 920
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