Tag | Content |
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EnhancerAtlas ID | HS128-01800 | Organism | Homo sapiens | Tissue/cell | MCF-7 | Coordinate | chr1:204732420-204733660 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
TBX20 | MA0689.1 | chr1:204733202-204733213 | CTTCACACCTA | - | 6.62 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| | Number: 1 | ID | Chromosome | Start | End |
GH01I204763 | chr1 | 204732729 | 204733387 |
| Enhancer Sequence | AAACTTCCAA TATGCCCACA GTGTGCTGAG TGCTTTTATG TCATTTTATT CTCCTAACCA 60 CCCACTATGG TAGGTATGGA ATCCCCCATT TTACTGATGA GGAAACTGAG GCAATGTATA 120 ACAGGTATAA GTAGCCCAAG GTTATTCAGG CACTAATGTG TAAGGCTGTG ATTCTAAGGC 180 AGACTGACTG ACTACAAAGC TAATGTTCTT AATCCCTAGA TGCTCCCACC TTCCAAATGT 240 CCTGGCTCCT AGAATTACAT CTGTTCTACT CCCTCCATGG CTCCATGGAA CCTGGACATC 300 TCAATTTCCT CCCCAAAAGC TGGAGTTCTC CAAGATGCAG AAGCCAGAGG GCTGATGTTC 360 CTGTGCAGGA AGAAGCAACG CCCAGGCCCA CTGCCCCCAC TCTCTCAGCA GATTCTCATT 420 TTCAGAATCC TGGAAACCAG AGCTAGAAAT CTGCCTCCCT CTGTTTACCC TGAGTTCCAA 480 TGTCACCAAC CCCCTTAATT AATGCTAGGG TGCTGGGTCA TGCATAGCAC GGTCAGCTTG 540 GTCTCCAGTT CTGGCAGCAG CTGCAGCCAA GGTCAAGAAC AACGGGGGCT GGGTTAGCTC 600 TTACTCATCC ACCTAAATGC CACTGCCCAC GCTCTCCGCT CTCGCCCCTC CCGCTGAGCA 660 GTGGCTGCCA GGGCGGCAGG AAGTCCTTCT TCCTGGGCCT GGCGCCCTCC AGCGGTGGGC 720 GCAGAGCACT AGGCTCCAAA ACTAGGAAGC CGGCTCAGCC TGCAGCAGGG CAGCTTGGGC 780 AGCTTCACAC CTAAACCAGC CTCTAAACGG GCGCACCTGG ACAAAACCCA GTAATTTAGA 840 AAAGCCTGTG TTTCTAGACA TCTCGCACTG CCAGCATTCT CCATGAGAAA GGAGCTAATA 900 GGATCAACTT TTCCTATACG CTGGAGACTT AATGAGTCCC TCACCGACCC AAGGCTGACC 960 TGTAATCTGA CAGATGACCA CGAAAAAGAG GCAATTTCAA GCCTAAAGAA AGGACCCCAT 1020 TATGTTGACA TTTAGGCATG AGTGTGGGTG GCATTGGGGC AGGAGTCCTA TGTGCTGCTC 1080 AAATCCCACC GTAGAGTCAA CTGGCAGTGT GGCCTCTGTC TGACACAGCT CAGGCTCTCC 1140 TGCTCCGAGG GAGTTTAGCA GAAGGTCCCT TACCCCACCC AGTTCTGCAG CCCCTCTGAG 1200 AAGTCACATA GCTGATGCCC ATGGGGGCTG GCGGTGTGCC 1240
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