Variant report
Variant | rs10167720 |
---|---|
Chromosome Location | chr2:209866395-209866396 |
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] |
---|---|
rs10178837 | 0.91[EUR][1000 genomes] |
rs10186320 | 0.84[AMR][1000 genomes];0.92[EUR][1000 genomes];0.87[ASN][1000 genomes] |
rs10192840 | 0.92[EUR][1000 genomes];0.81[ASN][1000 genomes] |
rs10497912 | 0.89[EUR][1000 genomes] |
rs10497913 | 0.91[EUR][1000 genomes] |
rs10497914 | 0.91[EUR][1000 genomes] |
rs10497915 | 1.00[CEU][hapmap];0.91[EUR][1000 genomes] |
rs10497916 | 1.00[CEU][hapmap];0.82[GIH][hapmap];0.86[MEX][hapmap];0.95[TSI][hapmap];0.90[EUR][1000 genomes] |
rs10497917 | 1.00[CEU][hapmap];0.82[GIH][hapmap];0.86[MEX][hapmap];0.95[TSI][hapmap];0.91[EUR][1000 genomes] |
rs1107012 | 1.00[CEU][hapmap];0.82[GIH][hapmap];0.95[TSI][hapmap];0.91[EUR][1000 genomes] |
rs11884061 | 0.84[AMR][1000 genomes];0.92[EUR][1000 genomes];0.81[ASN][1000 genomes] |
rs11884074 | 0.92[EUR][1000 genomes];0.81[ASN][1000 genomes] |
rs12464172 | 0.90[EUR][1000 genomes] |
rs12991020 | 0.90[EUR][1000 genomes] |
rs13007238 | 0.89[EUR][1000 genomes] |
rs13018777 | 0.88[EUR][1000 genomes] |
rs13019486 | 0.92[EUR][1000 genomes] |
rs13021774 | 0.89[EUR][1000 genomes] |
rs13022155 | 0.91[EUR][1000 genomes] |
rs13024347 | 0.91[EUR][1000 genomes] |
rs13025032 | 0.91[EUR][1000 genomes] |
rs13025499 | 0.99[EUR][1000 genomes] |
rs13026927 | 0.84[EUR][1000 genomes] |
rs13029761 | 0.91[EUR][1000 genomes] |
rs13411078 | 0.81[AMR][1000 genomes];0.92[EUR][1000 genomes];0.83[ASN][1000 genomes] |
rs1357247 | 0.91[EUR][1000 genomes] |
rs1357248 | 0.83[AMR][1000 genomes];0.92[EUR][1000 genomes];0.82[ASN][1000 genomes] |
rs1402996 | 0.83[AMR][1000 genomes];0.96[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs1402999 | 0.91[EUR][1000 genomes] |
rs1522201 | 0.91[EUR][1000 genomes] |
rs1522202 | 0.84[AMR][1000 genomes];0.91[EUR][1000 genomes];0.83[ASN][1000 genomes] |
rs16842022 | 0.91[EUR][1000 genomes] |
rs16842024 | 0.91[EUR][1000 genomes] |
rs16842028 | 0.91[EUR][1000 genomes] |
rs16842029 | 0.91[EUR][1000 genomes] |
rs16842030 | 0.91[EUR][1000 genomes] |
rs16842036 | 0.91[EUR][1000 genomes] |
rs16842052 | 0.91[EUR][1000 genomes] |
rs16842053 | 0.91[EUR][1000 genomes] |
rs16842199 | 0.93[EUR][1000 genomes] |
rs16842268 | 0.96[EUR][1000 genomes] |
rs16842299 | 0.94[EUR][1000 genomes] |
rs1818784 | 0.84[AMR][1000 genomes];0.92[EUR][1000 genomes];0.83[ASN][1000 genomes] |
rs1829708 | 0.90[EUR][1000 genomes] |
rs1851368 | 0.91[EUR][1000 genomes] |
rs1949689 | 0.96[EUR][1000 genomes] |
rs1969381 | 0.95[EUR][1000 genomes] |
rs2364697 | 0.88[AMR][1000 genomes];0.92[EUR][1000 genomes];0.87[ASN][1000 genomes] |
rs2886146 | 0.90[EUR][1000 genomes] |
rs2886148 | 0.92[EUR][1000 genomes];0.81[ASN][1000 genomes] |
rs34227926 | 0.91[EUR][1000 genomes] |
rs34326398 | 0.95[EUR][1000 genomes] |
rs34578232 | 0.90[EUR][1000 genomes] |
rs35179183 | 0.91[EUR][1000 genomes] |
rs35245441 | 0.91[EUR][1000 genomes] |
rs35251783 | 0.91[EUR][1000 genomes] |
rs3851939 | 0.91[EUR][1000 genomes] |
rs3851940 | 0.91[EUR][1000 genomes] |
rs3851941 | 0.91[EUR][1000 genomes] |
rs3863854 | 0.88[AMR][1000 genomes];0.92[EUR][1000 genomes];0.83[ASN][1000 genomes] |
rs3914935 | 0.90[EUR][1000 genomes] |
rs3914937 | 0.91[EUR][1000 genomes] |
rs4109419 | 0.91[EUR][1000 genomes] |
rs4366838 | 0.91[EUR][1000 genomes] |
rs5002645 | 0.91[EUR][1000 genomes] |
rs56335750 | 0.90[EUR][1000 genomes] |
rs58821250 | 0.95[EUR][1000 genomes] |
rs66515766 | 0.90[EUR][1000 genomes] |
rs6717179 | 0.85[AFR][1000 genomes];0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs71409838 | 0.92[EUR][1000 genomes];0.80[ASN][1000 genomes] |
rs72989312 | 0.87[EUR][1000 genomes] |
rs73064322 | 0.91[EUR][1000 genomes] |
rs7559978 | 0.91[EUR][1000 genomes];0.80[ASN][1000 genomes] |
rs7580198 | 0.92[EUR][1000 genomes] |
rs7588985 | 0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs7599045 | 0.92[EUR][1000 genomes];0.80[ASN][1000 genomes] |
rs7606381 | 0.92[EUR][1000 genomes] |
rs883049 | 0.92[AMR][1000 genomes];0.96[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs939848 | 0.94[EUR][1000 genomes] |
rs9646841 | 0.97[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs9989816 | 0.82[AFR][1000 genomes];0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];0.91[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv460058 | chr2:209755059-209866395 | Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS | TF binding regionCpG islandChromatin interactive region | 2 gene(s) | inside rSNPs | diseases |
2 | nsv584306 | chr2:209755059-209866395 | Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats | TF binding regionCpG islandChromatin interactive region | 2 gene(s) | inside rSNPs | diseases |
3 | nsv1012184 | chr2:209755847-210049331 | Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Strong transcription Bivalent Enhancer Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 7 gene(s) | inside rSNPs | diseases |
4 | nsv536131 | chr2:209755847-210049331 | Enhancers Weak transcription Strong transcription Bivalent Enhancer ZNF genes & repeats Genic enhancers Flanking Active TSS Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 7 gene(s) | inside rSNPs | diseases |
5 | esv3487576 | chr2:209768379-209947296 | Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Flanking Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 3 gene(s) | inside rSNPs | diseases |
6 | esv3487577 | chr2:209768379-209947296 | ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 3 gene(s) | inside rSNPs | diseases |
7 | nsv1009924 | chr2:209805661-210042572 | Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Active TSS Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 6 gene(s) | inside rSNPs | diseases |
8 | nsv875760 | chr2:209817526-209929978 | Enhancers Bivalent Enhancer Weak transcription ZNF genes & repeats | Chromatin interactive regionlncRNA | n/a | inside rSNPs | diseases |
9 | nsv1002578 | chr2:209836205-210026339 | Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 3 gene(s) | inside rSNPs | diseases |
10 | nsv536132 | chr2:209836205-210026339 | Bivalent Enhancer ZNF genes & repeats Weak transcription Enhancers Genic enhancers Active TSS Flanking Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 3 gene(s) | inside rSNPs | diseases |
11 | nsv526239 | chr2:209864064-209877078 | Weak transcription Enhancers ZNF genes & repeats | n/a | n/a | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr2:209865200-209868800 | Weak transcription | H1 BMP4 Derived Trophoblast Cultured Cells | ES cell derived |
2 | chr2:209866000-209868400 | Weak transcription | Placenta Amnion | Placenta Amnion |