| Tag | Content |
|---|
EnhancerAtlas ID | HS047-13776 |
Organism | Homo sapiens |
Tissue/cell | Fetal_placenta |
Coordinate | chr17:2952020-2952880 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Foxo1 | MA0480.1 | chr17:2952845-2952856 | AGTAAACAGGA | - | 6.32 | | Myod1 | MA0499.1 | chr17:2952592-2952605 | GGCAGCTGTCCCC | + | 6.29 |
|
| | 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 |
| GH17I003048 | chr17 | 2951632 | 2953094 |
|
Enhancer Sequence | CCAGGACGAT TTCGCTCCCC GGTGGACGTG GAGGGCGGGC AGGGTCATCC TTTCTCCTGA 60
AACTGGGGAG CCCTACGAAG GGGTTCCGGA GAAGACGCAC GGATCTCGAA TACCTCCCCG 120
CCCGGCTGCC ACTGGATGGC GCGCGCAACC TGCGGAACCA CAGGGCGACA TCCAGCTGCG 180
GGCGGCGAAG GGAATTGGAG CGTGGACCTC TCCAGGCTTT TCATTCGCTG GTTCTGCCGG 240
TGTCCCGCCT TTTCCATCTC CTCATTGGCT GTCGCCTCCG GGCCTGCGAC TTTGCTCAGC 300
CCCTCCGGGG AGTGGAATCG GGTGTGCAAC AGGCCGTGAG GTCCGGCTTT GCGAGGAACT 360
CCCATTGGTC AGTCAAACAG GAGTCCCACC CTCCTGGGCT TCCCATTGGT TGCTGTCCCA 420
CCGCTGCTCT CAGTTTCCCA GCGGCTGGGG ATCTGGGTTT TCTGGGGGTG GAGGGGTGCA 480
GTACGCTGCT GGAAGCTCGT TTCTCTTTCC ACCGTTGTGT GCCTCGGGCT CGCGGTCAAC 540
GGGGCTGGAC GAGGTTCAGA ACCCTCCAGA GCGGCAGCTG TCCCCGGGGT GGGTTGTGGG 600
ACTCAACAGC CCTCAGGGGA AAATGGCGGG AGGCAGGTGG AGGTGTCTTC TTTGCACTGA 660
AGACCTGGAT ACCCTGCTGC GGGCTGAACG GGAGGCTGGG GTGGAGCCCT GGCTCGGGTT 720
ATGGCCGGGG AGGAGACCAC GCTGGGCGAG TGGGAGGCAG CCCCAGCCAG GGGCTGGAAG 780
ACCAAGTACC GGACCTTCAA GGGCCTTCTT GCACCCGCAT CCCACAGTAA ACAGGATACG 840
TAGGTGACCG TCTAGAAAAC 860
|
