Tag | Content |
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EnhancerAtlas ID | HS047-33906 |
Organism | Homo sapiens |
Tissue/cell | Fetal_placenta |
Coordinate | chr9:34158080-34159080 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOXP2 | MA0593.1 | chr9:34158550-34158561 | TTTGTTTACTT | - | 6.62 | KLF5 | MA0599.1 | chr9:34158632-34158642 | GCCCCGCCCC | + | 6.02 | Nfe2l2 | MA0150.2 | chr9:34158539-34158554 | AGCTGAGTCATTTTG | - | 6.13 | Nr5a2 | MA0505.1 | chr9:34158892-34158907 | CTTGACCTTGGACTT | - | 6.29 |
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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 |
GH09I034157 | chr9 | 34157931 | 34159519 |
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Enhancer Sequence | CTGGGCAACA TAGCAAGATC CCTGTCTCTA CAAAAAACTA AAAAATTAGC TGGGCATGGT 60 GGTGCATGCC TGTAGTCACA GCTACTCTGG AGGCTGAGGC AGAAGGATCA CTTAAGTCCC 120 AGAATTTGAG GCTGCAGAAA GTTATGATTG GGCCAGTACA CACCAGCCTC AGCGACAGAG 180 CAAGACTCTG TCTCTCTCTC TCTTTTTTTT TTTTTAGCAA AATCAAAAAA ATTTTAAATG 240 TCGGCAAGAA TACAGCAAAA CAGCTACCTT CATACACTTT GGTTCCAGTG TAAAGAAATC 300 TGTTTGACAC GCAATTTGGA GAAATGGGGA AGCTGTGGTG AATGGGAATT CATGGCCCTG 360 GACCTACAAA AAGCCTGCAT TCCTGCCAGT ATGGCTACTT TGTTCATGTG CGCACTGTGC 420 CTGCTCTGGG GGGGTTAATG ACACAGGCTA TCATCAACTA GCTGAGTCAT TTTGTTTACT 480 TGGCTGTTCA GTGCCTCTTA TGTGGTGCAT TCTCTCTGGT ATGCCTTAAC ATGTTGTTAC 540 GAACTGAATT GTGCCCCGCC CCTCCAAGTT CTTATGTTGA AGTCCTAACC ACCCCACTTA 600 CCTCAGAATG TGACTGTATT TGGAGAAAGG GCCTTTAAGT AGGTGATTAA AGATCCTAAT 660 GCAATCTGAC TGGAGGCCTT ATAAGGAAGA AATCTGGACA CACAGAGATA CCAGAGACGT 720 GAGTGCACAG AGAAAAGGCA TAGAGTTGAG GATACAGTGA GAAGGCGAAA GCTAAGGAGA 780 GAGGCCTGAG AAGAAACCAA ACCTCCTGAC ACCTTGACCT TGGACTTCTG GCCTCCAGAA 840 CTGTGAGAAA ATAGATTTAC ATTGTTTAAT CCATCCAGTC TATAGTATTT TGTTATGGCA 900 ACCCTAGCAA ACAAATACAC ATGTGATACA AAGATCTTCA TACTCATGCC CCTTCCTATA 960 TGTTCACTTG GAATTCTTTG TCCTTAGATC TCCTTATTCC 1000
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