| Tag | Content |
|---|
EnhancerAtlas ID | HS121-23264 |
Organism | Homo sapiens |
Tissue/cell | LNCaP |
Coordinate | chr2:242002320-242003000 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Myod1 | MA0499.1 | chr2:242002346-242002359 | GGTGACAGCTGCA | - | 6.5 | | Myog | MA0500.1 | chr2:242002349-242002360 | GACAGCTGCAG | + | 6.62 | | TFAP2A | MA0003.3 | chr2:242002373-242002384 | TGCCTGAGGCA | - | 6.02 | | Tcf12 | MA0521.1 | chr2:242002349-242002360 | GACAGCTGCAG | + | 6.14 |
|
| | 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 |
| GH02I241063 | chr2 | 242002571 | 242005641 |
|
Enhancer Sequence | GGTAAGAGGG GCCCTGGCCC CGCTGGGGTG ACAGCTGCAG CACACTGGCC ATGTGCCTGA 60
GGCACTGGGT CCCCCGGACA GGTCTCTGTC TGGATGGCCA GGGTGGCCAC TGCATGCTTT 120
CTCGGGCCCC TGCCAGCTCT GACATCCAAG ACAAAGATTT TACAAATATC CCTTCCTGCA 180
CCTCCCCAGG GGAGACTGAG AGCCCAGCTG AGAAATGCTG GCCTGGCTTC AGGGCGCAGA 240
GAAGGTGGGC GTCGGAGAGG GCAGGTCACA GTCTCTGACA CCTGGTCGGT GCTTCCAGCC 300
AGTGGAGGGA GGGGAGGCCT GCCCCATGAG CCCTGCACAC TCTTGTACCT CGCTAGGGCT 360
CTAAGCCTGA GAAACGCAGG CTCCAGGGAG GGCAAGGCCC AGGGAGCCGT GCCCAGTCGT 420
GGCCCTGGGG AGCCTCCCAT TGCGGAGTGG CCTGGAGGAA GGCATGGCCT GGAGGTGGGG 480
CTTTGCCAGC AGGCAGTGGA GGTGGCACGC CTCCCGAGGA GGGGTGGGTT TGGGGCTGAT 540
GGAAGAAAAA GCACATGTCC TGAGTAGTTG CTCCCAGCTG GGAAAGGGGT AACTGAAGCC 600
CCAGGAAATG CACGGAATCC TGGGGGCATG TGGGCGCCTC AGACTTGAGC CAGCAACACC 660
CTTGACACCC CTTCTCTGTG 680
|
