| Tag | Content |
|---|
EnhancerAtlas ID | HS184-12269 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr16:28288890-28289830 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| RREB1 | MA0073.1 | chr16:28289650-28289670 | CCCCACCTCACCCACCCCGC | + | 6.86 | | Sox3 | MA0514.1 | chr16:28289669-28289679 | CCTTTGTTTT | + | 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 |
| GH16I028277 | chr16 | 28288521 | 28290030 |
|
Enhancer Sequence | GATCGCATGA GCCCAGGAGG TGGAAGCTGC AGTGAGCCAT GATCACACCT CTGCACTCCA 60
GCCTGGGCGA CAGTGAGACC CTTTCTCCAA AATACAAATT TTAAAAGGTA CTCTGGGGCT 120
GGCACAGACC GGGGACCTCG AGTGGACCAG CTGGGGAGGG GATTCATGTC CTGGGTTGTG 180
GGCGATCAGA AGATGGAAAT GTCGTGGTCT TGCCCTCGAG AACCAGATAG AACAGAGACA 240
GAGACAGAGC GCGCGCCGCG GTCCCTCAGA TCGTCCTGCA CTACGGCGAA ACGGCCACTA 300
GAGGGCGTGT TGTGCTCACA TATGCGGACC GGCCGGCAAG CGGCGGATTC CGCGGACAAA 360
GTCTCTTGTT TAGCCACAGA ACCCTGGGCT TGGCCCCAGG CCCGCTACGT CCGGGCCGTG 420
TGGCCTCAGC CAGGTTACAC AAAAGCTCTG TGACCCTGTT TGGTCAGCCA TAAAATGGGC 480
ACAGCTATAA GTCCGACCTT CTAAGGTGGT GTGAGGATGC CCGAGGCCAC GCAGGCAGAG 540
CAGCGTCCAG TGGGGAACGA ATGGCCCCGC GAGAAGGGGA GGCTTCGCCA TGGCCTCCGT 600
CTCTCTCCGC TTCTCCTGCA GCTCCTCCGC CCAGCCCTCC CCAGGCCACA TCCGGTCCCG 660
GGAGAGAGAC TGAGATCGAC TTTGGGGCAG GGGAGAGCAG GGGGAGGTAG GCAGTGTCTA 720
GGACAGGGAA AGAGAGGAGG CAGCCACCTC CCTCACCCCA CCCCACCTCA CCCACCCCGC 780
CTTTGTTTTA GAGGCAGGAT CCTGCTCTGT CACCCAGGCT GGAGTGCAGT GTCCTGATCC 840
TGGCTCACTG CATCCTCAGC CTCCCAGGCT CAAGCGATCC TCCTGCCTCA GTCTTCTGAG 900
TAGCTGGGAC TACAGGCAGG TGTCACCACG CCTGAGAAAT 940
|
