Tag | Content |
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EnhancerAtlas ID | HS047-10391 |
Organism | Homo sapiens |
Tissue/cell | Fetal_placenta |
Coordinate | chr14:74684270-74685140 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Myod1 | MA0499.1 | chr14:74685110-74685123 | GGTGACAGCTGCA | - | 6.5 | Myog | MA0500.1 | chr14:74685113-74685124 | GACAGCTGCAG | + | 6.62 | Tcf12 | MA0521.1 | chr14:74685113-74685124 | GACAGCTGCAG | + | 6.14 | Znf423 | MA0116.1 | chr14:74684843-74684858 | GAAACCCAGGGGGCC | - | 6.02 |
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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 |
GH14I074217 | chr14 | 74684267 | 74685131 |
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Enhancer Sequence | GAGCCACCGC ACCTGGCCCA AGGAGGCACT TCCATTCGGA CAGACATACA AGTGAACGGA 60 CGGACGCTCC TAGGATGGGT GCTATGCATT GCTTAAGAAG GGGAACCTTT GAGGACCCTT 120 GAAATCCCTC CCCTCTGATG CCTTGGAGGA AGGCGGACTG GCCCAGATTC CCGGACCGGC 180 AACCGCCACC TGCCTCTCTG GTCTCCTCCC ACCCCGAGGG GATCGCGCTC GCGCCGCGCC 240 ACTCGCGCGG CCACCGCTAG AGGGAGCCGG GAGCGTCTCC GAAGTCTCCC GCTTGCGGCT 300 TCGCTCAGGC GCTGCCTTTC ACCCGCCTCG CAGGGGCTGC GAGGCTCCGA CAAGACTGGT 360 CCCTTCTTGT CATTAGGCCC TAGGCCCGCA GCCCTCCGCG GCCCCGACCT CTAGGAGGTG 420 CCCAGCACCA ACAGGCCGAC CCTATGCTCC CTACCCAGCC CTCCGCTATG AAAACCCTAA 480 CGCTGCTCTG CTACTGCCCC CATTTTACCA ATTAGGACAC AGAGAGGCTG ACAGATGTAC 540 CTAGGGTCAC ACAGCGAATG CGTGGCAGAG CCGGAAACCC AGGGGGCCTG GCTCCGAACC 600 CCCATGCCTC AGAGGATCTC AAGCACCTTC TTGTATCTTT CTGTTCAAGG GGAAACCGAG 660 GCACAGAGCA AGTCTAGAGC ATACTGTGTG GGTGGCCCAG TCTGCCAAGG ACCGACAGGA 720 GGCTAAAGCT AGGCGGCCAG CCCCTAGGCA GATGACCACA GCAGAAAAGC CTGTGGGGAG 780 AAGAGGTGCC AGCCTGCCCC AAGGTGGGGG TGGAGGGGGC TGTTGGTGCC TCCCAGGATG 840 GGTGACAGCT GCAGCCTTGG GTGGGAGGCC 870
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