Tag | Content |
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EnhancerAtlas ID | HS183-14473 | Organism | Homo sapiens | Tissue/cell | T47D-MTVL | Coordinate | chr9:139355720-139357330 | SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
| TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ZEB1 | MA0103.3 | chr9:139356831-139356842 | CCCACCTGCCC | + | 6.14 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr9 | 139356955 | 139357032 | chr9 | 139357218 | 139357317 |
| Enhancer Sequence | AGCATCCTGC AAAAGGCATT TCAGGGACCT TGGTGGGTTA TCGGCGGCGC TCACGTGACA 60 TGAGTCAAGA CAGGCCATGT GTCCTCACGC AGCAGCAGAT ACACAAACAA CCCAAAGGCC 120 TCAAAAACAC ACTTATTCAC CATTTGGAGA CTAAAGACAC GTAGCGATTC ATTATTTTCC 180 TGAGTTTCAA AGTCCCTGTG GTAGTGGGTA TTTGTAGATA TTTGCTGCTT TTATCCATTT 240 TCAGCATAAA ACACAAGCAC GCTAATCACA AACAGGGCTA ATCACGCAGC GCTGCCCACC 300 ACGCCGCCCC ATCCACTGGG AAACACGCTC GAGTCAACTC CCCAGTTCTA ACAGGAGGCC 360 TCCGCGAATA TCCTGTCAAC ACGGAGAGTG ACTCCAGTAA GGCAGCCTCC CCTTTCACCA 420 AAATCATCCA GGGCATAATT TAGAACTTCT GGCTGGGAGG CAAAAACGTT ACAGTAGAGA 480 AAGATGTTAA TAAAAGCTAA CAGGTTACAT GACTTCAATC AGTTATAAAA CATCCATAAT 540 AGACTCATAC TGATCAGGCC GGGCGCGGTG GCTCATGCCT ATAATCCCAG CACTTTGGGA 600 GGCCAAGGTG GGCGGATTGC TTGAGCCCAG GAATTCGAGA CCAGCCTGGC AACATGGTGA 660 AACCCCGTCT CTACAAAAAA AAAAAAAAAG TTAGCCAGGC GTGGTGGCAT GCAGCTGTAG 720 TCCCAGCTAC TCAGGAGGCT GAGATGGGAG GATCACTTGA ACCCAGGAGG TCGAGGCCAC 780 ATTAAGCTGT GATCACGCCA CTGCACTCCA GCCTGGGCAA GAGTGAGACC CTGTCTCAAA 840 AAAAATTAAA AATAAAAAAA TAAAAATACT GGTCAAATAT GCCCTTTCTG AGTTTATCAT 900 GATATAAAAG GACAGAAAAC TCTCAGCCTA TCCCATGTCT CTGCTGTTCA GGGCCACACA 960 TGCTTCTGAG ACTGGCCTCT CTCCTGCTTA GCACATCCAA AGCAAACATC ATGCACCCTA 1020 GACAGCCCCT CCTGTGCACA TAGTGTCACT GCTGCAGTCA CTATGGACCC CCCAACCCCA 1080 CTGTCCCAGA GCAGGCTCCT GTCTCAGGCC CCCCACCTGC CCCAGTCCCC ACGCTGCTGT 1140 GACCCCAGTC ACTGGACGCT ACACGCACTG GCTGCTCTCT TGCCCATGGC CTTTCCATGC 1200 ACTGCGCCTC TGACAGGTTC AGTGTGCCCT CCCAACTCCC AATGACTTCT GGGCTGTGGA 1260 CTCGAGTCTG ACTTTGTGAG AATGCCACAA CTTGTGTCAT GCACATTTCA TCCGAGATTT 1320 GGCACACACA GCAGGGGCAC GGCCTGTGCT CAACATGTGC ATTTATCGAA TAACTGAAAA 1380 TTTAATCTGC AGGTCTCCAA CACTGGAAAC AGTTAGAAGG AAACCAACAT TAACACCTCC 1440 AGAAGGATGG CATACAAGAG TCAGGCATTG TTCAGGAAAC AGCAAGACCC GAAGCCCCAC 1500 ACTGCAGCGC GGATGCTCCC AAGAGGGGGC CACGTCCCTC CCTGAAGGCT GCAACCCCGC 1560 ACCAGGCCCG ACCCAGTGGA CATGTGCAGG CGCCAGGTGC CATGATGAGG 1610
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