Tag | Content |
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EnhancerAtlas ID | HS047-14309 |
Organism | Homo sapiens |
Tissue/cell | Fetal_placenta |
Coordinate | chr17:31263560-31264580 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CTCF | MA0139.1 | chr17:31264117-31264136 | TGCTGCCACCTGGTGGCTG | - | 7.88 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH17I032935 | chr17 | 31262182 | 31265119 |
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Enhancer Sequence | GGTGCACAGG CAACTTCAGC TATTTGTTTC CCACACATTT ACAGAGTGAC CAGGAGGGTT 60 TAGATACCGA GACTTCTCAG CTAAGGTGGG CTTCCACCAT CCCCACCTGC AGCATGACCC 120 ATCTGAGAGG GCTTTGGGGA AGCGCCAGCA GGTGCCTAGT CCTGACCCTG TCCTAGACCC 180 TGCCCTGCAG AGCCCGTGGC CGCCCCTCTT ACCCAGCCAC ATACCAGCTC CCCTTGACAC 240 GCCTTCCTCC CAGGCCAACA TGTCACACAG ATGCCCACAC CCCTGTCTCT GCCTGAATCT 300 GTGTTGGAGA CTAGCTTGGG GGACCCACTC TGGCTGTGCC CACTGCTCCA TCCCTGGCCC 360 AGGCCAGCAG CCTCCAGCAC TGGGTGGGAG CTGAAGCCAT ATGGCATTCA ACCTCCCAGA 420 TTCCAGGCTA ACTGCGAAAT CCCGTGTGGG AGGCAACCAG CAGGATTGCA GTCAACAGCT 480 ACACCCCCTC ATTTGGGCTT GATATCGTGA GGAAAAATAA AGCCCTTTTC TTAGAGCCAA 540 GGGCTGTACT AAGTTTGTGC TGCCACCTGG TGGCTGGTAT GCCGACGTGC CTGAGCAGAG 600 GGTCGGGGCC AGGATGTTTT CCACGTCAGC CACCTGGCCC CTCCGCCCAC CCGGGAGGGC 660 ACCTCTGTAT GCCTGCTGAA ACAATGGCAC TGCTGTGAGT TCCAGGGGCC CACACGTTCC 720 TTGTTGCCAT GGCCCCAGGT AAATCACGAG GAACCAGCCC TTTCTCTGCC TCAAGATTAA 780 CCAAATAAAA ACGACCAGTT TCCTGAGTTG CCACGTGAGT TCCTCTGAGG GAATACACGA 840 CCTGGTCAGC TTGAACTCAG TCCAGGCAGT TCAGTGAGTT GAGAGAGTGG GAGGGAGATA 900 ATCCAGGGAG GGACTCAGCT GAGAACAGTT CCCTGCCTTC TCTGGAATTG CCTCCAGTGG 960 GCTGTAGCCA CATGGTCAGC CCCTGGCTTT ATAAGAACCC ACATCCCAGG CTCTGGGTGG 1020
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