Variant report
Variant | rs10741105 |
---|---|
Chromosome Location | chr10:26231128-26231129 |
allele | A/G |
Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:0)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
No data |
No data |
No data |
No data |
No data |
No data |
No data |
rs_ID | r2[population] |
---|---|
rs10741103 | 0.86[ASN][1000 genomes] |
rs10764588 | 0.83[ASN][1000 genomes] |
rs10764589 | 0.81[ASN][1000 genomes] |
rs10764590 | 0.87[ASN][1000 genomes] |
rs10764591 | 0.87[ASN][1000 genomes] |
rs10764594 | 0.89[ASN][1000 genomes] |
rs10764595 | 0.88[AFR][1000 genomes];0.87[AMR][1000 genomes];0.96[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs10764597 | 0.81[EUR][1000 genomes] |
rs10828897 | 0.83[ASN][1000 genomes] |
rs10828907 | 0.86[ASN][1000 genomes] |
rs10828912 | 0.89[ASN][1000 genomes] |
rs10828913 | 0.89[ASN][1000 genomes] |
rs10828915 | 0.84[AMR][1000 genomes];0.95[EUR][1000 genomes];0.92[ASN][1000 genomes] |
rs10828916 | 0.90[ASN][1000 genomes] |
rs10828917 | 0.90[ASN][1000 genomes] |
rs10828922 | 0.83[AFR][1000 genomes];0.92[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs10828927 | 0.87[ASN][1000 genomes] |
rs10828928 | 0.87[ASN][1000 genomes] |
rs10828940 | 0.89[EUR][1000 genomes];0.84[ASN][1000 genomes] |
rs10828942 | 0.88[EUR][1000 genomes];0.82[ASN][1000 genomes] |
rs10828943 | 0.87[EUR][1000 genomes];0.80[ASN][1000 genomes] |
rs10828947 | 0.85[EUR][1000 genomes] |
rs10828948 | 0.82[EUR][1000 genomes] |
rs11014850 | 0.81[AMR][1000 genomes];0.94[EUR][1000 genomes];0.89[ASN][1000 genomes] |
rs11014851 | 0.86[ASN][1000 genomes] |
rs11014863 | 0.87[ASN][1000 genomes] |
rs11014913 | 0.88[ASN][1000 genomes] |
rs11014937 | 0.87[EUR][1000 genomes] |
rs12241971 | 0.92[EUR][1000 genomes];0.89[ASN][1000 genomes] |
rs12268184 | 0.83[EUR][1000 genomes] |
rs12570908 | 0.89[ASN][1000 genomes] |
rs12570917 | 0.86[ASN][1000 genomes] |
rs12777444 | 0.90[ASN][1000 genomes] |
rs12779127 | 0.91[EUR][1000 genomes];0.82[ASN][1000 genomes] |
rs1339804 | 0.88[ASN][1000 genomes] |
rs1339805 | 0.84[EUR][1000 genomes] |
rs1339817 | 0.94[EUR][1000 genomes];0.89[ASN][1000 genomes] |
rs1416855 | 0.92[ASN][1000 genomes] |
rs1416859 | 0.92[EUR][1000 genomes];0.84[ASN][1000 genomes] |
rs1416862 | 0.82[AFR][1000 genomes];0.92[ASN][1000 genomes] |
rs1416863 | 0.83[ASN][1000 genomes] |
rs1474216 | 0.91[ASN][1000 genomes] |
rs1538645 | 0.89[ASN][1000 genomes] |
rs1578216 | 0.92[AFR][1000 genomes];0.87[AMR][1000 genomes];0.99[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs1578217 | 0.89[EUR][1000 genomes];0.82[ASN][1000 genomes] |
rs1851146 | 0.85[ASN][1000 genomes] |
rs1915477 | 0.89[EUR][1000 genomes];0.81[ASN][1000 genomes] |
rs1976828 | 0.88[EUR][1000 genomes];0.82[ASN][1000 genomes] |
rs2027356 | 0.86[ASN][1000 genomes] |
rs2153345 | 0.91[ASN][1000 genomes] |
rs2204023 | 0.89[ASN][1000 genomes] |
rs2367988 | 0.82[ASN][1000 genomes] |
rs2368116 | 0.86[ASN][1000 genomes] |
rs2368117 | 0.94[EUR][1000 genomes];0.92[ASN][1000 genomes] |
rs2368121 | 0.85[EUR][1000 genomes] |
rs2947353 | 0.89[ASN][1000 genomes] |
rs3006270 | 0.86[ASN][1000 genomes] |
rs3737275 | 0.86[ASN][1000 genomes] |
rs3758450 | 0.89[ASN][1000 genomes] |
rs3824699 | 0.86[EUR][1000 genomes] |
rs4328138 | 0.86[ASN][1000 genomes] |
rs4403709 | 0.87[EUR][1000 genomes] |
rs4503431 | 0.86[ASN][1000 genomes] |
rs4747545 | 0.87[EUR][1000 genomes] |
rs4749083 | 0.86[ASN][1000 genomes] |
rs4749084 | 0.96[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs6482520 | 0.91[ASN][1000 genomes] |
rs6482523 | 0.92[AFR][1000 genomes];0.85[AMR][1000 genomes];0.95[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs6482524 | 0.83[AFR][1000 genomes];0.93[ASN][1000 genomes] |
rs7068085 | 0.91[ASN][1000 genomes] |
rs7069921 | 0.89[ASN][1000 genomes] |
rs7071420 | 0.86[ASN][1000 genomes] |
rs7071526 | 0.89[ASN][1000 genomes] |
rs7073804 | 0.89[ASN][1000 genomes] |
rs7074489 | 0.89[AFR][1000 genomes];0.85[AMR][1000 genomes];0.94[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs7077072 | 0.82[EUR][1000 genomes];0.84[ASN][1000 genomes] |
rs7083201 | 0.81[ASN][1000 genomes] |
rs7084310 | 0.89[ASN][1000 genomes] |
rs7084614 | 0.87[EUR][1000 genomes] |
rs7100118 | 0.83[ASN][1000 genomes] |
rs7100134 | 0.88[ASN][1000 genomes] |
rs7100527 | 0.85[EUR][1000 genomes];0.89[ASN][1000 genomes] |
rs7896398 | 0.94[EUR][1000 genomes];0.84[ASN][1000 genomes] |
rs7904360 | 0.96[EUR][1000 genomes];0.89[ASN][1000 genomes] |
rs7905199 | 0.89[ASN][1000 genomes] |
rs7908158 | 0.90[ASN][1000 genomes] |
rs7908742 | 0.92[ASN][1000 genomes] |
rs7914361 | 0.89[ASN][1000 genomes] |
rs7914935 | 0.84[ASN][1000 genomes] |
rs7918880 | 0.89[ASN][1000 genomes] |
rs7920650 | 0.85[ASN][1000 genomes] |
rs7921074 | 0.81[ASN][1000 genomes] |
rs7923264 | 0.92[ASN][1000 genomes] |
rs7923691 | 0.86[AFR][1000 genomes];0.95[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs8181447 | 0.87[ASN][1000 genomes] |
rs9299814 | 0.82[ASN][1000 genomes] |
rs9645527 | 0.83[ASN][1000 genomes] |
rs9663248 | 0.96[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs9664363 | 0.90[ASN][1000 genomes] |
rs9665611 | 0.85[ASN][1000 genomes] |
rs9731571 | 0.85[ASN][1000 genomes] |
rs993397 | 0.89[ASN][1000 genomes] |
rs993398 | 0.89[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv894974 | chr10:26028530-26322783 | Weak transcription Enhancers Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 8 gene(s) | inside rSNPs | diseases |
2 | nsv1051756 | chr10:26092320-26277478 | Enhancers Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 8 gene(s) | inside rSNPs | diseases |
3 | esv3390154 | chr10:26230678-26231161 | Weak transcription | n/a | n/a | inside rSNPs | n/a |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr10:26229800-26233600 | Weak transcription | hESC Derived CD184+ Endoderm Cultured Cells | ES cell derived |