Tag | Content |
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EnhancerAtlas ID | HS047-17725 |
Organism | Homo sapiens |
Tissue/cell | Fetal_placenta |
Coordinate | chr19:45995470-45996410 |
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) |
HNF4G | MA0484.1 | chr19:45995499-45995514 | TGACCTTTGTACCCC | - | 6.07 | IRF1 | MA0050.2 | chr19:45995797-45995818 | AAAAAGAAAAAGAAACTTTAG | - | 6.15 | Zfx | MA0146.2 | chr19:45995571-45995585 | GAGGCCGAGGCGGG | - | 6.01 |
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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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Enhancer Sequence | CTCCTAAACC CAACCTCAGC CCTGACCAGT GACCTTTGTA CCCCAACCTT CATCTCATCT 60 GTCTAAACTT TAGGCTCACT CCTGTAATCA CAACACTTTG GGAGGCCGAG GCGGGAGGAT 120 CACCTGAGGC CTGGACAACA TAGTGAGACC CTGTCTCTAC AAACAAAATA AGAAAATTAG 180 CAGGGCGTGG TGGCCTGTGG CTCTAGTCCC AACTACTTGG GAGGCTGAGG TGGGAGGATC 240 ACTTGTGCCC AGGTGTTGGA GGCTGCAGTG AGCTATGATC CCACCACTGC ACTCCAGAAA 300 GGGCGACAGA GGGAGACTCT GTGGCTTAAA AAGAAAAAGA AACTTTAGTA ATCTGCTTTC 360 CTTTGAGTCC TGAAAACCAG GAACTCAGTA CCTTTCTATT TCTTTCCAGA TCCTCTCTAT 420 CCTCCCACAC TCCCTCCAAC TGACCCCTCC GACCGGTCCC TCTTAGAGGC TCACCCCTCA 480 CTTCCGTCTC CTTCCAATGC ATCTCCTCTC ATTTACCTCC AAATAGGGCA GCCCCTCCCT 540 CCCCATAGCA GGGCCCTCCC AGGCAGGCTC CTAGTGGCCG GCGCCGGTGG ATGGGGGAGG 600 GGCCAGGTCG CCTGAGGCGG GGGCTAAGTT TAGGCACGCT GGGGGGAGGG GGCCTCCCCG 660 CAGCTGTTCT GGCCCGTCTG GCCCCTGAGT GACAGCGCTG CCTGGGGCCG AGGCTGGGGG 720 AGGGGGTCCT CCCTGCTCCT GGGCCCCAAA GTGCTGGCTC GAAGGAGAAG GGACCCCATG 780 CTCCCTCTGG GTCCTCCCTA TACTGCCCCT CGGCCCCCTA GCCCCAGCCT GCAGCGCTGC 840 GGAAGCAGAT CAGTAATAAA AATGCTCCGG ATGTGCAGGA GATAAGGGCG AGTTTGGACC 900 CCGTTCCGCC GACCTCAGCC CCCGTCCAGC CCGTTCCGCA 940
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