Tag | Content |
---|
EnhancerAtlas ID | HS183-01915 |
Organism | Homo sapiens |
Tissue/cell | T47D-MTVL |
Coordinate | chr16:89312880-89313930 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
KLF16 | MA0741.1 | chr16:89313912-89313923 | GGGGGCGGGGC | - | 6.02 | KLF5 | MA0599.1 | chr16:89313913-89313923 | GGGGCGGGGC | - | 6.02 | SP1 | MA0079.4 | chr16:89313911-89313926 | CGGGGGCGGGGCCTG | - | 6.11 | Zfx | MA0146.2 | chr16:89313912-89313926 | GGGGGCGGGGCCTG | + | 6.19 |
|
| 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 |
GH16I089246 | chr16 | 89312961 | 89315287 |
|
Enhancer Sequence | ACATATACAC CATGGAATAC TATGCAGCCA TAAAAAAGAA GCGAGATCAT GTCCTTTGCA 60 GGCACATGGG TGGAGCTGCA AGCCATTATC CTCAGCAAAC TAACGCAGGA ACAGGAAAGT 120 AAACACGGCA TGTTCTCACT TATAAGTGGG AGCTGAACAA CATGAGCACA TGGACACAGG 180 GAGGGGAACA AAGCACACTC GGGCCTGTTG GGGGAGGGCG GGGGCAGGAG GGCATTAAGA 240 AAAATAGCTA ATGCATGTCC GGCTTCATAC CTACGTGACG GGTTGATAGG TGCAGCAAAC 300 CACCATGGCA CACGTTTACC TATGCAACAA GCCTGCACAT CCTGCACGTG TACCCCAGAT 360 ATTAAAAAAA ATAAATACAT CCGACGTTTC GTGAAAGCTG ACTGGGCATT AGTGGATCCA 420 AGCACCAAAC AGGACGGCAG GTGGAGACGT GGGACAGAGG CGGGTGGAGA GAGAAGCCGG 480 CGGGATCCAA GGCCCCAGGG CAGGCCCTGG CAGCGATGTG GCAGCCCCTC TGCAGTTTCC 540 ACGCTGGTAG TCGTGAAGTA AATTCTAGGC CCTGCTCCCC AACCGGCGCG GGCCGCCCTC 600 GCCTTCAGCT CCAATGCTGC TGCGCCCCAG GCCGCCCCGC TCCTGGCAGG CCCCAGCCTC 660 TGACTCAGCC CCCCGCCTAG CCCCTGAGAG CAGCCTCTCC GCGGGACTGG CCTGTGCGCG 720 CGCGTCTGCG GCACCGTCGG ACCAGGGGCC GCCCCCGAGC GGGGAGCCCA GGAGGACGGC 780 CAGGTGGCCT GAGGCAGAGG CGCCAGGGAG GATGGAGAAG GGACACCCAG GGCCTAGGCG 840 GGGTGGGGGC AGGGAGGGCG GCGGGACAGC AAGGAAGTGG GTGCACCTGG GTGACCCAGC 900 TGCGCATGAG CGGGCAGGGG CTCGGGGCGC GCGGACTCCA GGCGCTGGAC TGCGGCGTGG 960 AGCAGCGCTG GGGAAACCGC GCCGGGTTCA GCGAGGATTG CTGGGCGGGG CGCGCGAGGA 1020 GCGAAGCTGG CCGGGGGCGG GGCCTGAGTC 1050
|