Tag | Content |
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EnhancerAtlas ID | HS183-09968 |
Organism | Homo sapiens |
Tissue/cell | T47D-MTVL |
Coordinate | chr7:73020440-73021300 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
IRF1 | MA0050.2 | chr7:73020746-73020767 | TTTTTCTTTTTCTTTTTTTTT | + | 6.09 | Nr2f6(var.2) | MA0728.1 | chr7:73020512-73020527 | AGGGTCAAGTGGTCA | + | 6.3 | Zfx | MA0146.2 | chr7:73020999-73021013 | CCCGCCTCGGCCTC | + | 6.01 |
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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 |
GH07I073606 | chr7 | 73021044 | 73022121 |
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Enhancer Sequence | CCTAGGGAGA CAGAGCCGTC AGCAGCCGCT AGAGAGCTCC CACTGCCCCG ATCTTCCATA 60 TCACCCCTCT CCAGGGTCAA GTGGTCAGCA GGACAGAGGG TCTGTCTGTT CACACCTCTG 120 TCACCTTTCC CTAGTGGACC TAGCTTGCTG CTTGAAAGGC CAAGATCACT CCATTGGCCT 180 CTAAGAACTT CCCCCAGGAG ATAGACCAGG ATGCAGATAC AGGGGTCCCC TTCCTGCTCT 240 TTAGATTTTT TCCTGTCTGG GACCCCAGTT CTTTGGTCCC TCTGGTTTTT TTTTTTGTTT 300 GTTTTCTTTT TCTTTTTCTT TTTTTTTTTT TTGGAGACGG AGTCTCACTC TGTTGCCCAG 360 GCTGGAGTGC AGTGGCGCAA TCTCAGCTCA CTGCAACCTC CACCTCCCAG GTTCAAGCGA 420 TTCTCCTGTC TCAGCCTCCT GAGTAGCTGG GATTGCAGGC ATGCGCCACT ATGCCCGGCT 480 AATTTTTGTA TTTTTAGTAG AGACGGGGTT TCACCATGTT GGCCAGGCTG GTCTCGAACT 540 CCTGACCTCA GATGACCCAC CCGCCTCGGC CTCCCAAAGT GCTGGGATGA CAGGCGTGAG 600 CCACCACGCC CGGCCTGGTC CCTCTGTTCT CCCATGCCTC CCACCACTTG CTCAATGACC 660 TGGGGTCTTC TCACCACCTC ACCCTCACCC CCCAAGAAGA GAAGAGCTCA ACAAATGAAC 720 CACAGGATGG CAGTAACATC CCACATTCCA CCCTCATGCC CAGCCACTGT CTTGCCCACT 780 GAGGCGGAAA CTGTCAACTC TGCCTCCCAT CTACTTGGGG GGCAAAGGGA TGCCCTTGCC 840 TGCTGGACTT ACAGAGCACC 860
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