Tag | Content |
---|
EnhancerAtlas ID | HS047-06344 | Organism | Homo sapiens | Tissue/cell | Fetal_placenta | Coordinate | chr11:67440510-67441900 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Zfx | MA0146.2 | chr11:67440644-67440658 | CCCGCCTCGGCCTC | + | 6.01 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | CCTGCCTCAG CCTCCCGAGT AGCTGGGACT ACAGGTGCCC GCCACCACAC CCAGCTTATT 60 TTTTGTGTTT TTAGTAGAGA CGGGGTTTCA CCGTGCTAGC CAGGATGGTC TCGATCTCCT 120 GACATCGTGA TCCGCCCGCC TCGGCCTCCC AAAGTGCTGG GATTACAGGC AAAATAAACT 180 TTATAAATTA ACTGAGACCC GTCTCAGATT TTCTGGGTTT ACACTGGGGA CCTCTGGCTG 240 CTCACCAGGC AGTTCCTGAC TGGACCTGGG TCCCATAGGT GACCACCCCA GACTTGGCCA 300 GCCCCCATGG AGCTCACAGT CTACACACGG AACAATGACA CCGGAAACAA TATCATTACA 360 AACATGATCG GTGGGCCAGG GCTTCTTCCA GAGGTGGCCA GAGACCCACC CCTGGCTCTG 420 ACTGCTGCGG GGAAGCCGTA GGGGAGGGCC TCTTGGAGGG CAGGTGATCT GGACAGAGGG 480 ACCAACGTGT GCAAAAGCCC TGTGGGGGCA GATGCTGAGA AATAAGACAC ACAGGAAGGT 540 GGAGGCCTGA TGGGACCTGT CATATGGAGA GGGGACTCAT TCCCTTGGCA GTGGCCATGC 600 CTGGTGCAGG GCCCAGAAAG AAGTCAGAGC TGGCATCTGG GGCCAGGTAG CTGGCATGCA 660 CATCTCATCT GAGCCTCACA GCTATTATTA TTACCCAGTT GGAAGGACAG GGAAACCGAG 720 GCTCCCAGAG ACGACTTGAT TTGCCCTCCT CACAGCCTCA GTGCGAGGAG GGAGGCCCCC 780 CAGCCCCTCT CCTCACACCA GCCTTGTGAC ACCATGTGCC AATGTGTGCC TCGTGCCTTT 840 CACTGTCTTC TCAACATCTT CCTGCAGCTT CCAGACTTTC TAAATGCGAA TGTAGTATTT 900 CTAGAACCAG AAACAAGCAA TGCATGTTGC TTTTAACATC TGAAACCAAA GATCCGACTT 960 TCGCTTCAAC TGCCAAGAAT CTCTCTGCTT CCAATCCCCG ATTCTCCGGC ACCTCCTGAT 1020 CACAGCCCTG GTGCCCCCGA CCCAATCCTT GTCTGTCCAC AGAGCTGCCT TCTCCTCTAA 1080 CCTGGGAGCT CCTCAAAGGG AGGACGGGGT CTGTCCCCAT CCCTGGGGCT CCTGGGGAAC 1140 AGGCTTCATT TCTGTGGCTG CTTCCCAGGA GCCTGCCAAA GGGCAAAGTG AGGCTCAGAA 1200 GACACCAGCA CCCACCTCCC TCTCCTGAGC AAGCCCCGTA CCCATGGCCC CTGCAGCCAT 1260 AGGCCCCTTG GTGGGCTTGC CCCCTGACCC ACGGGCCATG GGCACACATC CCCTTCCCTC 1320 CATGCCCCTG GTTCCCACCA GTGTCCTTTA CCCTGAGCTC CCTCTGCCCG CCCCTCACCC 1380 CTGTGGCCCC 1390
|
| |
|
|
|