Tag | Content |
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EnhancerAtlas ID | HS184-10361 | Organism | Homo sapiens | Tissue/cell | T47D | Coordinate | chr14:76177340-76178820 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
MEOX1 | MA0661.1 | chr14:76178146-76178156 | GCTAATTAAC | + | 6.02 |
| | 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 |
GH14I075711 | chr14 | 76177399 | 76179832 |
| Enhancer Sequence | ACAGAAAGAT TAAATTCATT TCACAAGACA GTTTTGTGAT ATAAGTTATT TTGTGTAAAA 60 TTTTTTAACA CAAAATTAAA TTCGTGAAAA CCCTAGTTTC TGTATAGATG AGTGTTTTCA 120 GTTGTCCTTA TTGTTTTATT AACATAAGAA GTGGGAGAGC TCTCACTGTT TTCTCATGTG 180 TGGGTATAGT ATTGAAGAAG TGTTGCAATT GTCCCCCTGG TATTTGGGTG CAGCTTTTTG 240 TGATTCCCAC AGTAGCCCTC AGAGGTCCCC TGTGCTTTTG AATTTTACTT GCGTGTTGCT 300 GTTTTGCACC ACCAGGGGAC ACTCAGTTTC CACAGAGGGG TGCTATGCTC TACCAAAATG 360 GTGCAGATTC TTTTTCCTGT CAGGGGTGGA CTCCAAAAAG ATTTTGTCCT GGATTTTACA 420 GCTTTAGGTG GATCCAGTAT TGGGTTTAGA TGAGTTGACA GAGCCCTTTC TGAGATGAAG 480 CTAATAGCCA GATTTTCACT GAAACAGGAA AAATAAAAAT TTCAAAAAAA TTAAAACAAA 540 ATGGAGTTAA AAACTAAATA TGTTGCCAGA GACCCAAAGA TAGGCAGCTC TAGCAACTTG 600 GGGGGCATGC AAGTATCCAT CCAGGGAGCT GAGTTCCACC CATGCGGCGG AGGTGGGAAG 660 AGAGGATTCT GGGAAGGTCC CGGTTGGAAT GGCCTTTTTT CTGCCTCAGC CATATTATTC 720 AGTGGAAATT CAGAAAAGAC CCCAAAACAT TTGTAGTGCC TTTCCCTTTC TCCCCACCCC 780 CAGTTCCTTC TTCAGTAGCC TTCCTTGCTA ATTAACACTG GCTCTGCAGG GATATTTACC 840 TTTTCTCTGC TGGATTCCTG TGGTTTTGAA AGAATTCAGG TACTTGCTGG TTGCCAAGGA 900 ATTCAGATTA CCTCACAGGC TGCACACTGT CCAGAATCTG CCACAGCAGC AAGTAGGGGG 960 GAAGAGACAC CAACAAGGGG GAGAAAACCC TTTCCAGTGC TCATTGTCAC CCTCCCTGGC 1020 AGGCCCTTGC TGTTTGTGAA GTTTGAGTCA TTTCTGGCTC TAAAGACAAG GGATCAGGCT 1080 GGTAATCCCC TCCCAGACGG CTCTGTAGGG CGCTGCCTAG TCACTGCAGC GCTTTGGCAG 1140 TCTCCCGGCT GCAGCTGGTT GACAGCAGAT CAGAGAGCTC TTGGGCCTCT TGTTCTCTTC 1200 CATAAGATTT TTCTGGGTCA GGCCAGGATG AAACCCAGTG GCTCCTGGCA AGGCTGCCTG 1260 AGGTGCTGTC TCTTCATTGT CCAGGCCTCT CTGACTCAAA ATGCCTACAC CTGTTGAAGG 1320 ATAACTCATG TGCCACAGCG AGGTCGAGGC TGGCCTTCTC TTTTCTTGGT ACATTTGTAG 1380 TGAATGTTTG TCAGAAAATA TAACTACCAA AGAGGATGTT AAGCTTCTAC ATCTAGAATG 1440 CCTGTGACTC TGACCATAAG AAGATATTGG TATCAAAAAA 1480
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