Variant report
Variant | rs72836518 |
---|---|
Chromosome Location | chr10:116763984-116763985 |
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] |
---|---|
rs10160015 | 0.90[ASN][1000 genomes] |
rs10444099 | 0.95[ASN][1000 genomes] |
rs1045657 | 0.83[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs10510008 | 0.81[ASN][1000 genomes] |
rs10885632 | 0.81[ASN][1000 genomes] |
rs10885633 | 0.95[ASN][1000 genomes] |
rs10885634 | 0.95[ASN][1000 genomes] |
rs10885636 | 0.95[ASN][1000 genomes] |
rs10885637 | 0.95[ASN][1000 genomes] |
rs10885638 | 0.95[ASN][1000 genomes] |
rs10885639 | 0.95[ASN][1000 genomes] |
rs11196983 | 0.81[ASN][1000 genomes] |
rs11196984 | 0.81[ASN][1000 genomes] |
rs11196989 | 0.81[ASN][1000 genomes] |
rs11196991 | 0.95[ASN][1000 genomes] |
rs11196996 | 0.95[ASN][1000 genomes] |
rs11196999 | 0.95[ASN][1000 genomes] |
rs11197000 | 0.95[ASN][1000 genomes] |
rs11197005 | 0.95[ASN][1000 genomes] |
rs11197006 | 0.87[ASN][1000 genomes] |
rs11197007 | 0.95[ASN][1000 genomes] |
rs11197010 | 0.95[ASN][1000 genomes] |
rs11197011 | 0.95[ASN][1000 genomes] |
rs11197012 | 0.95[ASN][1000 genomes] |
rs11197023 | 0.84[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs12098332 | 1.00[ASN][1000 genomes] |
rs12246008 | 0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs12265048 | 0.81[ASN][1000 genomes] |
rs12269261 | 0.95[ASN][1000 genomes] |
rs12764662 | 1.00[ASN][1000 genomes] |
rs12772737 | 0.81[AFR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs12774597 | 0.94[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs12779231 | 0.85[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs17092671 | 0.84[AMR][1000 genomes];0.92[EUR][1000 genomes] |
rs17721905 | 1.00[ASN][1000 genomes] |
rs17722042 | 0.83[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs17795104 | 0.86[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs17795212 | 0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs2095379 | 0.95[ASN][1000 genomes] |
rs2105001 | 0.95[ASN][1000 genomes] |
rs2420070 | 0.81[ASN][1000 genomes] |
rs34170154 | 1.00[ASN][1000 genomes] |
rs34200762 | 0.87[AMR][1000 genomes];0.89[EUR][1000 genomes] |
rs34318200 | 0.94[AMR][1000 genomes];0.94[EUR][1000 genomes] |
rs34434610 | 1.00[ASN][1000 genomes] |
rs34453431 | 0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs34461950 | 0.91[ASN][1000 genomes] |
rs35501899 | 1.00[ASN][1000 genomes] |
rs35811923 | 0.84[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs3931556 | 0.95[ASN][1000 genomes] |
rs61869271 | 1.00[ASN][1000 genomes] |
rs61869272 | 0.81[AFR][1000 genomes];0.83[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs61869274 | 0.81[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs61869275 | 0.84[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs61869297 | 0.80[EUR][1000 genomes] |
rs6585302 | 0.81[ASN][1000 genomes] |
rs6585306 | 0.95[ASN][1000 genomes] |
rs6585309 | 1.00[ASN][1000 genomes] |
rs6585310 | 1.00[ASN][1000 genomes] |
rs6585311 | 1.00[ASN][1000 genomes] |
rs6585313 | 1.00[ASN][1000 genomes] |
rs7071789 | 1.00[ASN][1000 genomes] |
rs7071812 | 0.95[ASN][1000 genomes] |
rs7079234 | 0.87[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs7085964 | 0.90[ASN][1000 genomes] |
rs7086663 | 0.80[EUR][1000 genomes] |
rs7087420 | 0.81[EUR][1000 genomes] |
rs7090904 | 0.80[EUR][1000 genomes] |
rs7093282 | 0.87[ASN][1000 genomes] |
rs7093330 | 1.00[ASN][1000 genomes] |
rs7097580 | 0.97[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs7099565 | 0.95[ASN][1000 genomes] |
rs7099590 | 1.00[ASN][1000 genomes] |
rs7099779 | 0.95[ASN][1000 genomes] |
rs7100026 | 0.82[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs7100159 | 0.95[ASN][1000 genomes] |
rs7100894 | 0.81[ASN][1000 genomes] |
rs769119 | 0.80[EUR][1000 genomes] |
rs7898249 | 0.95[ASN][1000 genomes] |
rs7904605 | 0.95[ASN][1000 genomes] |
rs7908069 | 0.95[ASN][1000 genomes] |
rs7908464 | 0.95[ASN][1000 genomes] |
rs7917523 | 0.95[ASN][1000 genomes] |
rs881192 | 0.95[ASN][1000 genomes] |
rs968848 | 0.83[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs968849 | 0.86[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv949138 | chr10:116311531-116874477 | Weak transcription Strong transcription Enhancers Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 21 gene(s) | inside rSNPs | diseases |
2 | nsv1038050 | chr10:116315109-116895719 | Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Strong transcription Bivalent/Poised TSS Active TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 21 gene(s) | inside rSNPs | diseases |
3 | nsv533027 | chr10:116344641-116856352 | Weak transcription Enhancers Active TSS Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 21 gene(s) | inside rSNPs | diseases |
4 | esv3435429 | chr10:116394152-117006347 | Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription Strong transcription Genic enhancers Flanking Active TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 21 gene(s) | inside rSNPs | diseases |
5 | nsv831996 | chr10:116601552-116772968 | Weak transcription Enhancers Strong transcription Genic enhancers Active TSS Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 11 gene(s) | inside rSNPs | diseases |
6 | nsv1039002 | chr10:116643095-116879483 | Active TSS Enhancers ZNF genes & repeats Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 10 gene(s) | inside rSNPs | diseases |
7 | esv2761634 | chr10:116643095-116879495 | Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Active TSS ZNF genes & repeats Genic enhancers Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 10 gene(s) | inside rSNPs | diseases |
8 | nsv1045654 | chr10:116654574-116879483 | Weak transcription Active TSS Flanking Active TSS Enhancers Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 10 gene(s) | inside rSNPs | diseases |
9 | nsv1043242 | chr10:116655057-116883386 | Enhancers Strong transcription Flanking Active TSS Weak transcription Bivalent/Poised TSS ZNF genes & repeats Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 10 gene(s) | inside rSNPs | diseases |
10 | nsv831997 | chr10:116689552-116855698 | Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 9 gene(s) | inside rSNPs | diseases |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr10:116761800-116764200 | Enhancers | Ovary | ovary |
2 | chr10:116762200-116766600 | Weak transcription | HSMMtube | muscle |
3 | chr10:116763400-116764800 | Enhancers | Fetal Brain Male | brain |
4 | chr10:116763600-116766600 | Weak transcription | Fetal Adrenal Gland | Adrenal Gland |