Tag | Content |
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EnhancerAtlas ID | HS183-08758 | Organism | Homo sapiens | Tissue/cell | T47D-MTVL | Coordinate | chr7:4821380-4822940 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
MYC | MA0147.3 | chr7:4822479-4822491 | CGGCACGTGGCC | - | 6.52 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr7 | 4822384 | 4822539 | chr7 | 4822544 | 4822598 |
| Enhancer Sequence | CCCAGGTAGC GCAGCAGTCA CCACCCCAGT TGGCACCGGA TGGCTGCTTC CCAAGGAACA 60 GGGGAGACAG GAAGCAGGGG CGCCAGAGCC GGCAGGTGGC TGCTTGTTGT AGACGCATCT 120 CGGTGCTGAG TGCCTGGCAC ACTTGAGGCT GGGGCATGCC CTGTTGACTG GAACGGGGTC 180 CCATGCCCAG CAGGCCCACG TGGTATGTTG GTGCTCAGGA GAGGTGGTGG AGTTTGGTTT 240 CTCAGACAGA GCCTTGAGAC AGCGAGTCAG TGGAGGCTGG GCCTCCAGAC CTTCTTTTTG 300 GGGTTTTTGT TTTGTTTTTT AGAAACAGGG TCTCACTCTG CTGTCCAGTG TAGAGTGCCA 360 TGGAGTGATC AATGCTCACT GCAGCCTCGA CCTCCCTGGC TCAAGCAATC CTCCCATCTC 420 AGCCTCCTGA GTAGCTGGGA TTACAGGCAT GCATCACCAC ACCCAGTTAA TGTTTGTATT 480 TTTTTGTAGG GACCTGGGGT CTCACTATGT TGCCCAGGCT GGTCTCAAAC TTCTGGGCTC 540 AAGCAATCCA CCCTCCTTGG CCAGGAGTTT TTGCCAAGTC CATGTCCTCC CTCCCTCTGT 600 GTCGGGAGCA GGCCTGGGCA CTCAGCGTGG GGATCCAGGG GTTCACAGGC TGCCTTTGTG 660 TGAGAGAAGC TGCTATCTCT GCTCATGGGT TGCCCAGGGG TGCAGAGTCT GCAGGAAGGT 720 TGCGATGGAG CTGGGCTTTT CCCTCCGTTC CCAGCCTGCA GCGTCATGAG TTGCCTCCTG 780 TGCTGGGGTG CAGCCTGCGG TTGCTTTAGT TCTGTGTGGG CGAGAGCTTG TGGGCCCCGG 840 CGTACTCAGG GCGTTGTACT TCATCACTGG GGTCATCCTG GTTGGTGCCC AGCCCCCTCA 900 CCTCACAGAC CTCCTGCAGG CCACCTCCAG GCCTCCGAGA TGACCCCGGT AATGCTGTGG 960 TAGCTCCTGG CCTTTGGAAC AAGATGACTC CGGCTCTTCT TGTTTGTTTC ACCCGCCCTT 1020 CTCCTCAAGC AACTCATTTT TTTCAGTGGA AGATGATCTT GCAGAACTGC TGCCAGGCGC 1080 CAGCGGTGCA CCCCCCGCCC GGCACGTGGC CTCCCAGCCA CCCAGCCGCC CTCCTCCCTG 1140 CCCTGACGGC CCTGCCCCTG TGCTGGGTGT CTCTGGTGCT GCTCAGATGT TTCAGCACCT 1200 GGGTGTGCAG AGTGAGGTGG GTGGTTTAAA GACTGGGATC CACACTGGAG GCCCCGCAGG 1260 ACGGGGTGTC CTGTGTCTGC GGCCAGGGCC ATGGTGGCCG CCAGTGTGTT TTTAGCATTG 1320 AATCAGCCGT GCCCTCACCC AGGCCCCCTC CAGCCTCAGC GATGCAGCTC CCAGGGAGAG 1380 AGGCTGGAGG CGGAGCAGGC ACCTTGTGGC CCGGGGTGGG CCTGCGCGGG ACATCCTCCC 1440 TGCCACCTGC TAGGCCGGGG TCTCAGCGAC CGACGCTTCT CAGGAGTGTC ACACAGACTT 1500 CCGAAATGGG GGAGCTGGTC TCTGGCACAG GCCAGTACCC CAGCGTTTGC CCTGTTTGAT 1560
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