| Tag | Content |
|---|
EnhancerAtlas ID | HS047-14159 | Organism | Homo sapiens | Tissue/cell | Fetal_placenta | Coordinate | chr17:25707620-25708610 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr17:25708204-25708223 | CCTCGCCCCCTGGTGGCGG | - | 6.42 |
| | | 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 |
| GH17I027379 | chr17 | 25706728 | 25708654 |
| Enhancer Sequence | AGTCTTATGG TCTCTGTTTT TAGATGGTGT CACAAGGCTC AGAGAGGGTA AATGAAGAGC 60
CCGAGGTCAC CCAGCTTGTA GGTAGCAGAG CGGGGATGCT CCTCACCCTG CACGGAGCAG 120
CCTGTAGCAT CATAAGCTGT TGCTTGCCCT GACGTGGGGA GCCAGGGGGA TGGCGGACTT 180
CTCAGGTTCG TTTCTCTGCC CACACCTGGC AGGCTGTCCC TGAAAGCTGT CCTCTTTCAT 240
CATTTATTCA GCCATTCATC CATTCATTCC TGAGCATTCG AGGCTGCGTG CTGAACCCTG 300
GGGGACCACA GTGAACAAGC TAGATACCAC CCTTCCTGCG AAGAGCTCGA GGCCAGTGGG 360
GGTCCCTAAG GAGAGCCGGG AACATCAAAC CTGCGGATTG GGAGTAAATA TTAAATCCAG 420
TTCCTCTCCC CGATTTACAT GCACACACAC GCACCCGCAC AGTCCCTTCA TCTTCTGAGT 480
GTCATGGGAA CGGGGACTTC TAGCCCTCGG CGGTGGCCAG CAGCACTGGC AGCCGCCCAG 540
CCGCAAGGGG ACGCTGTGAG GGCAGCGAGC AGGATTCCCT AGGCCCTCGC CCCCTGGTGG 600
CGGCAGCGGC TCCTGCTCTG CTCACCACGC CCCTCGGTGA TTTCTGGCCC TCCCCCGCCC 660
CGGTTGAGCC TCTTGGGGGC CTCTTGGGTC ACCACTTCTC TCCCTTCCTG TTCCAGCCCT 720
GTGGGGAGGG CCTGTTGGCC TTCACCTAGG CCATGCCCTG GTGTTGCCAC AAAGCGCCTT 780
GGAGGCCGTA TCTCACCAGC CGGCAGGAGG TCCCTGCATC AGGCCTGGGC CTCAGACACA 840
TTCTCTCCTG TGATCCTCTA GCCAGCCTCT CCCCCGTCCC CCCTTCTGAT GAGCCAAAGG 900
TTCTGCGCCA TGCATGCTCA AGCTGGGACT GCCGCTGTCC TGGACAGAGA CCAGCTCTAA 960
ATCAGGCAAT TTAGAGCCAG GCGTGGTGGC 990
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