Variant report
Variant | rs9823218 |
---|---|
Chromosome Location | chr3:110562705-110562706 |
allele | A/T |
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] |
---|---|
rs1020891 | 1.00[EUR][1000 genomes] |
rs1037960 | 1.00[EUR][1000 genomes] |
rs1160101 | 1.00[EUR][1000 genomes] |
rs11929276 | 1.00[EUR][1000 genomes] |
rs1350928 | 1.00[EUR][1000 genomes] |
rs1350931 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs1381827 | 0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs1381829 | 1.00[EUR][1000 genomes] |
rs1462297 | 1.00[EUR][1000 genomes] |
rs1462312 | 1.00[EUR][1000 genomes] |
rs1462791 | 1.00[EUR][1000 genomes] |
rs1462792 | 1.00[EUR][1000 genomes] |
rs1462796 | 1.00[EUR][1000 genomes] |
rs1462806 | 1.00[EUR][1000 genomes] |
rs1546533 | 1.00[EUR][1000 genomes] |
rs1580287 | 1.00[EUR][1000 genomes] |
rs1599575 | 1.00[EUR][1000 genomes] |
rs1599577 | 1.00[EUR][1000 genomes] |
rs1599665 | 1.00[EUR][1000 genomes] |
rs1841734 | 1.00[EUR][1000 genomes] |
rs1849369 | 1.00[EUR][1000 genomes] |
rs1903758 | 0.95[AFR][1000 genomes];1.00[EUR][1000 genomes] |
rs1960628 | 1.00[EUR][1000 genomes] |
rs1975901 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs1993781 | 1.00[EUR][1000 genomes] |
rs1993801 | 1.00[EUR][1000 genomes] |
rs2054376 | 1.00[EUR][1000 genomes] |
rs2061682 | 0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs2169566 | 0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs3957571 | 1.00[EUR][1000 genomes] |
rs3957572 | 1.00[EUR][1000 genomes] |
rs4305447 | 1.00[EUR][1000 genomes] |
rs4333116 | 1.00[EUR][1000 genomes] |
rs4549301 | 1.00[EUR][1000 genomes] |
rs4593059 | 1.00[EUR][1000 genomes] |
rs4682021 | 1.00[EUR][1000 genomes] |
rs4682216 | 0.83[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs4682218 | 0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs4682220 | 1.00[EUR][1000 genomes] |
rs58412853 | 1.00[EUR][1000 genomes] |
rs61035297 | 1.00[EUR][1000 genomes] |
rs6437932 | 0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs6437935 | 1.00[EUR][1000 genomes] |
rs6437936 | 1.00[EUR][1000 genomes] |
rs6766908 | 1.00[EUR][1000 genomes] |
rs6780526 | 1.00[EUR][1000 genomes] |
rs6781418 | 1.00[EUR][1000 genomes] |
rs6781884 | 1.00[EUR][1000 genomes] |
rs6794368 | 1.00[EUR][1000 genomes] |
rs6798353 | 1.00[EUR][1000 genomes] |
rs72935984 | 1.00[EUR][1000 genomes] |
rs72941202 | 1.00[EUR][1000 genomes] |
rs72943104 | 1.00[EUR][1000 genomes] |
rs72943107 | 1.00[EUR][1000 genomes] |
rs72943108 | 1.00[EUR][1000 genomes] |
rs72943110 | 1.00[EUR][1000 genomes] |
rs72943111 | 1.00[EUR][1000 genomes] |
rs72943114 | 1.00[EUR][1000 genomes] |
rs72943119 | 1.00[EUR][1000 genomes] |
rs72944942 | 1.00[EUR][1000 genomes] |
rs72944943 | 1.00[EUR][1000 genomes] |
rs72944949 | 1.00[EUR][1000 genomes] |
rs72944956 | 1.00[EUR][1000 genomes] |
rs72944965 | 1.00[EUR][1000 genomes] |
rs7609772 | 0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs7612471 | 1.00[EUR][1000 genomes] |
rs7615275 | 1.00[EUR][1000 genomes] |
rs7618482 | 1.00[EUR][1000 genomes] |
rs7619492 | 1.00[EUR][1000 genomes] |
rs7619978 | 1.00[EUR][1000 genomes] |
rs7628011 | 1.00[EUR][1000 genomes] |
rs7628921 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs7634788 | 1.00[EUR][1000 genomes] |
rs7639735 | 1.00[EUR][1000 genomes] |
rs7641366 | 1.00[EUR][1000 genomes] |
rs7642037 | 1.00[EUR][1000 genomes] |
rs7644614 | 1.00[EUR][1000 genomes] |
rs7650020 | 1.00[EUR][1000 genomes] |
rs898974 | 1.00[EUR][1000 genomes] |
rs9288915 | 1.00[EUR][1000 genomes] |
rs931024 | 1.00[EUR][1000 genomes] |
rs964444 | 1.00[EUR][1000 genomes] |
rs9818867 | 1.00[EUR][1000 genomes] |
rs9824638 | 1.00[EUR][1000 genomes] |
rs9826523 | 0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs9829084 | 1.00[EUR][1000 genomes] |
rs9830162 | 1.00[EUR][1000 genomes] |
rs9835919 | 1.00[EUR][1000 genomes] |
rs9856917 | 0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs9860353 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs9869379 | 1.00[EUR][1000 genomes] |
rs9874159 | 1.00[EUR][1000 genomes] |
rs988374 | 1.00[EUR][1000 genomes] |
rs990256 | 1.00[EUR][1000 genomes] |
rs992130 | 1.00[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv1010230 | chr3:110204439-110588814 | Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Active TSS Strong transcription Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 5 gene(s) | inside rSNPs | diseases |
2 | nsv536688 | chr3:110204439-110588814 | Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 5 gene(s) | inside rSNPs | diseases |
3 | nsv1003106 | chr3:110264476-111105943 | Weak transcription Enhancers Strong transcription Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 13 gene(s) | inside rSNPs | diseases |
4 | nsv1014199 | chr3:110293896-110754155 | Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Strong transcription Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 6 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr3:110556400-110587200 | Weak transcription | ES-WA7 Cell Line | embryonic stem cell |