Variant report
Variant | rs6672279 |
---|---|
Chromosome Location | chr1:73626527-73626528 |
allele | C/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] |
---|---|
rs10749815 | 0.98[AFR][1000 genomes];0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs10749816 | 0.89[EUR][1000 genomes] |
rs10789358 | 0.91[EUR][1000 genomes] |
rs10789359 | 0.89[EUR][1000 genomes] |
rs10889999 | 0.80[ASN][1000 genomes] |
rs10890011 | 0.92[EUR][1000 genomes] |
rs10890012 | 0.89[EUR][1000 genomes] |
rs10890013 | 0.89[EUR][1000 genomes] |
rs10890014 | 0.89[EUR][1000 genomes] |
rs10890015 | 0.89[EUR][1000 genomes] |
rs10890016 | 0.91[EUR][1000 genomes] |
rs11210114 | 0.81[EUR][1000 genomes] |
rs11210127 | 0.87[AFR][1000 genomes];0.87[AMR][1000 genomes];0.85[EUR][1000 genomes];0.89[ASN][1000 genomes] |
rs11210143 | 0.81[EUR][1000 genomes] |
rs11210155 | 0.89[EUR][1000 genomes] |
rs11210156 | 0.89[EUR][1000 genomes] |
rs11210157 | 0.89[EUR][1000 genomes] |
rs11210160 | 0.89[EUR][1000 genomes] |
rs11210161 | 0.89[EUR][1000 genomes] |
rs11210162 | 0.89[EUR][1000 genomes] |
rs11210163 | 0.89[EUR][1000 genomes] |
rs11210164 | 0.89[EUR][1000 genomes] |
rs11210165 | 0.89[EUR][1000 genomes] |
rs11210166 | 0.87[EUR][1000 genomes] |
rs11210167 | 0.87[EUR][1000 genomes] |
rs11210168 | 0.84[EUR][1000 genomes] |
rs11210170 | 0.92[EUR][1000 genomes] |
rs11210172 | 0.88[EUR][1000 genomes] |
rs11210174 | 0.90[EUR][1000 genomes] |
rs11582461 | 0.84[EUR][1000 genomes] |
rs11589897 | 0.84[EUR][1000 genomes] |
rs12033354 | 0.80[AMR][1000 genomes];0.85[EUR][1000 genomes];0.87[ASN][1000 genomes] |
rs12037338 | 0.92[EUR][1000 genomes] |
rs12059553 | 0.92[EUR][1000 genomes] |
rs12087611 | 0.90[EUR][1000 genomes] |
rs12122520 | 0.84[EUR][1000 genomes] |
rs12124553 | 0.84[EUR][1000 genomes] |
rs12126688 | 0.89[EUR][1000 genomes] |
rs12128855 | 0.84[EUR][1000 genomes] |
rs12136496 | 0.84[EUR][1000 genomes] |
rs12137298 | 0.88[EUR][1000 genomes] |
rs12143587 | 0.81[EUR][1000 genomes] |
rs12729632 | 0.80[ASN][1000 genomes] |
rs12742692 | 0.89[EUR][1000 genomes] |
rs12748124 | 0.80[ASN][1000 genomes] |
rs34548060 | 0.88[EUR][1000 genomes] |
rs34719239 | 0.89[EUR][1000 genomes] |
rs34868208 | 0.89[EUR][1000 genomes] |
rs34956095 | 0.89[EUR][1000 genomes] |
rs35133930 | 0.89[EUR][1000 genomes] |
rs35209284 | 0.88[EUR][1000 genomes] |
rs35286654 | 0.89[EUR][1000 genomes] |
rs35350320 | 0.88[EUR][1000 genomes] |
rs35446706 | 0.89[EUR][1000 genomes] |
rs35489458 | 0.89[EUR][1000 genomes] |
rs35578487 | 0.88[EUR][1000 genomes] |
rs36051652 | 0.89[EUR][1000 genomes] |
rs36053729 | 0.89[EUR][1000 genomes] |
rs36093886 | 0.80[ASN][1000 genomes] |
rs4294371 | 0.89[EUR][1000 genomes] |
rs4367754 | 0.89[EUR][1000 genomes] |
rs4391625 | 0.81[EUR][1000 genomes] |
rs4430278 | 0.93[ASN][1000 genomes] |
rs4477222 | 0.82[EUR][1000 genomes];0.86[ASN][1000 genomes] |
rs4492565 | 0.84[EUR][1000 genomes] |
rs4503305 | 0.88[EUR][1000 genomes] |
rs4537504 | 0.89[EUR][1000 genomes] |
rs4578169 | 0.87[EUR][1000 genomes] |
rs4579710 | 0.89[EUR][1000 genomes] |
rs4592219 | 0.88[EUR][1000 genomes] |
rs4593762 | 0.84[EUR][1000 genomes] |
rs4601539 | 0.88[EUR][1000 genomes] |
rs4607818 | 0.86[EUR][1000 genomes] |
rs4622012 | 0.82[EUR][1000 genomes];0.87[ASN][1000 genomes] |
rs4641264 | 0.83[EUR][1000 genomes] |
rs4650193 | 0.84[EUR][1000 genomes] |
rs4650194 | 0.84[EUR][1000 genomes] |
rs4650195 | 0.89[EUR][1000 genomes] |
rs4650196 | 0.84[EUR][1000 genomes] |
rs4650197 | 0.89[EUR][1000 genomes] |
rs61765598 | 0.87[EUR][1000 genomes] |
rs6424508 | 0.80[ASN][1000 genomes] |
rs6657881 | 0.89[EUR][1000 genomes] |
rs6657885 | 0.89[EUR][1000 genomes] |
rs6658012 | 0.88[EUR][1000 genomes] |
rs6666765 | 0.89[EUR][1000 genomes] |
rs6671028 | 0.89[EUR][1000 genomes] |
rs6674333 | 0.89[EUR][1000 genomes] |
rs6674404 | 0.89[EUR][1000 genomes] |
rs6683380 | 0.89[EUR][1000 genomes] |
rs6684331 | 0.89[EUR][1000 genomes] |
rs6686255 | 0.89[EUR][1000 genomes] |
rs6694634 | 0.89[EUR][1000 genomes] |
rs6695455 | 0.89[EUR][1000 genomes] |
rs6695460 | 0.89[EUR][1000 genomes] |
rs6696689 | 0.80[AMR][1000 genomes];0.85[EUR][1000 genomes];0.87[ASN][1000 genomes] |
rs6697098 | 0.89[EUR][1000 genomes] |
rs6698500 | 0.89[EUR][1000 genomes] |
rs6699861 | 0.85[EUR][1000 genomes] |
rs6700625 | 0.89[EUR][1000 genomes] |
rs6703953 | 0.91[EUR][1000 genomes] |
rs67437638 | 0.83[EUR][1000 genomes] |
rs7514409 | 0.87[EUR][1000 genomes] |
rs7519995 | 0.81[EUR][1000 genomes];0.80[ASN][1000 genomes] |
rs7526372 | 0.81[EUR][1000 genomes];0.80[ASN][1000 genomes] |
rs7545548 | 0.87[EUR][1000 genomes] |
rs7552256 | 0.81[EUR][1000 genomes];0.80[ASN][1000 genomes] |
rs9919151 | 0.81[EUR][1000 genomes];0.80[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv1005356 | chr1:73542786-74124065 | Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 7 gene(s) | inside rSNPs | diseases |
2 | nsv1010267 | chr1:73551169-73628431 | Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNA | 1 gene(s) | inside rSNPs | diseases |
3 | nsv870774 | chr1:73560811-73706449 | Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
4 | esv2757736 | chr1:73613099-73775684 | Enhancers Flanking Active TSS Weak transcription Active TSS | TF binding regionChromatin interactive regionlncRNA | 3 gene(s) | inside rSNPs | diseases |
5 | esv2758942 | chr1:73613099-73775684 | Enhancers Weak transcription Active TSS Flanking Active TSS | TF binding regionChromatin interactive regionlncRNA | 3 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr1:73626400-73626600 | Enhancers | Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells | embryonic stem cell |