Tag | Content |
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EnhancerAtlas ID | HS047-26805 | Organism | Homo sapiens | Tissue/cell | Fetal_placenta | Coordinate | chr5:42908380-42909420 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
KLF4 | MA0039.3 | chr5:42908664-42908675 | CCACACCCTGC | + | 6.62 | NRF1 | MA0506.1 | chr5:42909111-42909122 | GCGCATGCGCA | + | 6.32 | NRF1 | MA0506.1 | chr5:42909110-42909121 | TGCGCATGCGC | - | 6.32 | RREB1 | MA0073.1 | chr5:42909016-42909036 | GGTGTGGGGATGGTTTCGGG | - | 6.25 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | TCTTAACATG TAGTTTAAGT ATTACCCATT CCAGTGCTTC TCAGCCTTTA TTAGCATTTG 60 AAGATATTGT ACTTGTCTTC AGTTCTTCAA GGTAACTGCT GAGGCTGATT CTTTTCACAA 120 TGATTGTGGT TTCTTGAGTC AAAATAGTTT TTTTTCTGGG TCCTGAAGAC TATGTTTTGG 180 CTCTTGCTGC AACAGTAAGG GACTTGCAGT TCCCACTCTG TGCAGAGAAG TCTGTGGCCT 240 TGCAACTTTC CAGAGGGATC TATATATCCT TCCAACACAT CAACCCACAC CCTGCTCAGG 300 TTCGCAGGGC TTGGGTATTT GTGCATTGCA GCTGTTGTAA CAGTTTCCCA CGGGTGGTGA 360 AAGACGTGCT CTGCAGTCCA GATCTTGATG GTGCAGGCAG TCTGCTAGAT GTCTGTGAAG 420 CGCAGGGGAA AATGAGGTGA GGAGGCTACA CCTGTCCCAC CCCGTCGGGG GCCCTTCAAC 480 CAGCTTCGCT GTGCGCAGGT GCCGTCGGCT CCAAGTGAGG CGGTCCTCCA CTCTTCGTTA 540 CAATGTAACA TTTAAACCAT TTAAAGCAGA GATCCGCAAC GTTTTTGGCA CCAGGGACCA 600 GTTTAGTGGA ATACAATTTT TCTACGGATG GAGAGGGGTG TGGGGATGGT TTCGGGATGA 660 AGGTGTTAGA AATCAAATAA TCAGGCACGC AATAGATTCT CAAAAGGAGA GCAAAAGCTA 720 GTCTTGGTCC TGCGCATGCG CAGTTCACAA TAGGGTTCGC ACTCCTGTGA GAATTTAATG 780 CAGCAGATCT GACGCTAGGC GGAGCTCAGC CAGTAATGCT CGCTTGCCCA CTGCTCAGCT 840 CCTGCTTTGG GGCCGGGTTC CTAACCGGTC CGTGGTGGGG GGGATTGGGG ACCCCTGATT 900 TAAAGAACAG TGCTAATGCC TGTTTTCTGC CTTTATTTGG AGGGCCACAG TCAGTTTCAA 960 AGCAACTCCA GCATATGATC CACCCAGCTG TCCCCTCCCA CCCTGTTAGT ATCCACAGCT 1020 CCTCAAAGGC CCCTGGAATT 1040
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