Variant report
Variant | rs4333556 |
---|---|
Chromosome Location | chr8:104746639-104746640 |
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] |
---|---|
rs10089467 | 0.81[AMR][1000 genomes];0.84[EUR][1000 genomes] |
rs10093196 | 0.83[EUR][1000 genomes] |
rs10097250 | 0.96[AMR][1000 genomes];0.95[EUR][1000 genomes] |
rs10097397 | 0.96[AMR][1000 genomes];0.95[EUR][1000 genomes] |
rs10103621 | 0.83[AMR][1000 genomes];0.85[EUR][1000 genomes] |
rs10955321 | 0.91[ASN][1000 genomes] |
rs10955323 | 0.96[AMR][1000 genomes];0.95[EUR][1000 genomes] |
rs10955329 | 0.83[AMR][1000 genomes];0.85[EUR][1000 genomes] |
rs10955330 | 0.83[AMR][1000 genomes];0.85[EUR][1000 genomes] |
rs12216803 | 0.91[ASN][1000 genomes] |
rs12541306 | 0.83[AMR][1000 genomes];0.85[EUR][1000 genomes] |
rs12542880 | 0.97[ASN][1000 genomes] |
rs12543980 | 0.97[ASN][1000 genomes] |
rs12545944 | 0.97[ASN][1000 genomes] |
rs12546356 | 0.91[ASN][1000 genomes] |
rs12546553 | 0.88[ASN][1000 genomes] |
rs12547317 | 0.86[ASN][1000 genomes] |
rs12547819 | 0.97[ASN][1000 genomes] |
rs12548029 | 0.97[ASN][1000 genomes] |
rs12548742 | 0.97[ASN][1000 genomes] |
rs12549541 | 0.86[ASN][1000 genomes] |
rs13250282 | 0.96[AMR][1000 genomes];0.93[EUR][1000 genomes] |
rs13274021 | 0.91[AMR][1000 genomes];0.93[EUR][1000 genomes] |
rs1357015 | 0.96[AMR][1000 genomes];0.99[EUR][1000 genomes] |
rs1390848 | 0.83[AMR][1000 genomes];0.83[EUR][1000 genomes] |
rs1426297 | 0.91[AMR][1000 genomes];0.95[EUR][1000 genomes] |
rs1496845 | 0.82[EUR][1000 genomes] |
rs1521059 | 0.97[ASN][1000 genomes] |
rs1593497 | 1.00[AFR][1000 genomes];0.82[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs1607910 | 0.92[AFR][1000 genomes];0.80[AMR][1000 genomes] |
rs1607912 | 0.97[ASN][1000 genomes] |
rs16870503 | 0.86[ASN][1000 genomes] |
rs16870558 | 0.91[ASN][1000 genomes] |
rs16870578 | 0.91[ASN][1000 genomes] |
rs16870589 | 0.91[ASN][1000 genomes] |
rs16870611 | 0.97[ASN][1000 genomes] |
rs16870636 | 0.97[ASN][1000 genomes] |
rs16870649 | 0.97[ASN][1000 genomes] |
rs16870656 | 0.97[ASN][1000 genomes] |
rs16870733 | 0.97[ASN][1000 genomes] |
rs16870735 | 0.97[ASN][1000 genomes] |
rs16870772 | 0.97[ASN][1000 genomes] |
rs16870776 | 0.97[ASN][1000 genomes] |
rs16870788 | 0.85[ASN][1000 genomes] |
rs1820444 | 0.96[AMR][1000 genomes];0.93[EUR][1000 genomes] |
rs1893531 | 0.83[AMR][1000 genomes];0.84[EUR][1000 genomes] |
rs1895892 | 0.96[AMR][1000 genomes];0.95[EUR][1000 genomes] |
rs1895895 | 0.96[AMR][1000 genomes];0.93[EUR][1000 genomes] |
rs1948569 | 0.83[AMR][1000 genomes];0.84[EUR][1000 genomes] |
rs2047346 | 0.83[EUR][1000 genomes] |
rs2059587 | 0.96[AMR][1000 genomes];0.93[EUR][1000 genomes] |
rs2067550 | 0.97[ASN][1000 genomes] |
rs2080609 | 0.89[AMR][1000 genomes];0.85[EUR][1000 genomes] |
rs2080610 | 0.91[AMR][1000 genomes];0.85[EUR][1000 genomes] |
rs2080611 | 0.97[ASN][1000 genomes] |
rs2111493 | 0.95[AMR][1000 genomes];0.95[EUR][1000 genomes] |
rs2111494 | 0.97[ASN][1000 genomes] |
rs2114250 | 0.97[AMR][1000 genomes];0.96[EUR][1000 genomes] |
rs2160714 | 0.93[AMR][1000 genomes];0.93[EUR][1000 genomes] |
rs2388723 | 0.91[ASN][1000 genomes] |
rs28541426 | 0.96[AMR][1000 genomes];0.98[EUR][1000 genomes] |
rs28610511 | 0.83[EUR][1000 genomes] |
rs28806247 | 0.93[AMR][1000 genomes];0.94[EUR][1000 genomes] |
rs28883573 | 0.89[AMR][1000 genomes];0.87[EUR][1000 genomes] |
rs28890031 | 0.93[AMR][1000 genomes];0.93[EUR][1000 genomes] |
rs2892596 | 0.96[AMR][1000 genomes];0.93[EUR][1000 genomes] |
rs2935296 | 0.81[AMR][1000 genomes];0.84[EUR][1000 genomes] |
rs34195802 | 0.97[ASN][1000 genomes] |
rs35220144 | 0.82[EUR][1000 genomes] |
rs3956332 | 0.83[AMR][1000 genomes];0.85[EUR][1000 genomes] |
rs4301418 | 0.97[ASN][1000 genomes] |
rs4424225 | 0.83[EUR][1000 genomes] |
rs4532569 | 0.97[ASN][1000 genomes] |
rs4541867 | 0.94[ASN][1000 genomes] |
rs4549736 | 0.97[ASN][1000 genomes] |
rs4734081 | 0.97[AMR][1000 genomes];0.96[EUR][1000 genomes] |
rs4734719 | 0.91[AMR][1000 genomes];0.85[EUR][1000 genomes] |
rs4734733 | 0.83[AMR][1000 genomes];0.83[EUR][1000 genomes] |
rs55744580 | 0.91[ASN][1000 genomes] |
rs56139465 | 0.97[ASN][1000 genomes] |
rs56305252 | 0.86[ASN][1000 genomes] |
rs57079548 | 0.91[ASN][1000 genomes] |
rs57901487 | 0.97[ASN][1000 genomes] |
rs58596288 | 0.91[ASN][1000 genomes] |
rs58631312 | 0.97[ASN][1000 genomes] |
rs59382988 | 0.97[ASN][1000 genomes] |
rs59732166 | 0.97[ASN][1000 genomes] |
rs59802767 | 0.86[ASN][1000 genomes] |
rs59857402 | 0.91[ASN][1000 genomes] |
rs61099915 | 0.94[ASN][1000 genomes] |
rs61300996 | 0.91[ASN][1000 genomes] |
rs61556831 | 0.97[ASN][1000 genomes] |
rs6468883 | 0.96[AMR][1000 genomes];0.92[EUR][1000 genomes] |
rs6468892 | 0.82[AMR][1000 genomes];0.84[EUR][1000 genomes] |
rs6468894 | 0.97[ASN][1000 genomes] |
rs67138437 | 0.81[EUR][1000 genomes] |
rs67952889 | 0.95[AMR][1000 genomes];0.97[EUR][1000 genomes] |
rs6985834 | 0.97[AMR][1000 genomes];0.95[EUR][1000 genomes] |
rs6990561 | 0.97[ASN][1000 genomes] |
rs6991802 | 0.96[AMR][1000 genomes];0.93[EUR][1000 genomes] |
rs7001190 | 0.96[AMR][1000 genomes];0.93[EUR][1000 genomes] |
rs7003727 | 0.97[AMR][1000 genomes];0.96[EUR][1000 genomes] |
rs7007619 | 0.96[AMR][1000 genomes];0.98[EUR][1000 genomes] |
rs7011865 | 0.96[AMR][1000 genomes];0.91[EUR][1000 genomes] |
rs7462974 | 0.97[ASN][1000 genomes] |
rs7815399 | 0.96[AMR][1000 genomes];0.99[EUR][1000 genomes] |
rs7824905 | 0.96[AMR][1000 genomes];0.93[EUR][1000 genomes] |
rs7829854 | 0.81[EUR][1000 genomes] |
rs7832196 | 0.97[ASN][1000 genomes] |
rs7836355 | 0.97[ASN][1000 genomes] |
rs9297340 | 0.96[AMR][1000 genomes];0.98[EUR][1000 genomes] |
rs978825 | 0.97[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv429931 | chr8:104097396-104878014 | Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Transcr. at gene 5' and 3' Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent/Poised TSS Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNAmiRNA target site | 82 gene(s) | inside rSNPs | diseases |
2 | nsv1020476 | chr8:104312212-104924482 | Genic enhancers Enhancers Flanking Active TSS Active TSS Weak transcription Bivalent/Poised TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 42 gene(s) | inside rSNPs | diseases |
3 | nsv539704 | chr8:104312212-104924482 | Flanking Bivalent TSS/Enh Enhancers ZNF genes & repeats Weak transcription Active TSS Strong transcription Flanking Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 42 gene(s) | inside rSNPs | diseases |
4 | nsv1023048 | chr8:104355188-104872701 | Flanking Active TSS Strong transcription Weak transcription Active TSS Enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 39 gene(s) | inside rSNPs | diseases |
5 | nsv539705 | chr8:104355188-104872701 | ZNF genes & repeats Enhancers Strong transcription Bivalent/Poised TSS Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 39 gene(s) | inside rSNPs | diseases |
6 | nsv1021345 | chr8:104361854-104879684 | Enhancers Active TSS Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 39 gene(s) | inside rSNPs | diseases |
7 | nsv1032085 | chr8:104362187-104878345 | Active TSS Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 39 gene(s) | inside rSNPs | diseases |
8 | nsv1034183 | chr8:104369940-104814008 | Weak transcription Strong transcription Enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 38 gene(s) | inside rSNPs | diseases |
9 | nsv539707 | chr8:104369940-104814008 | Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Active TSS Bivalent/Poised TSS Enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 38 gene(s) | inside rSNPs | diseases |
10 | esv2752692 | chr8:104520824-105123824 | Enhancers ZNF genes & repeats Flanking Active TSS Weak transcription Strong transcription Active TSS Bivalent Enhancer Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 14 gene(s) | inside rSNPs | diseases |
11 | nsv1016387 | chr8:104578389-104931853 | Enhancers Weak transcription ZNF genes & repeats Active TSS Strong transcription Flanking Active TSS Bivalent Enhancer Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 6 gene(s) | inside rSNPs | diseases |
12 | nsv1031195 | chr8:104601231-105194208 | Enhancers Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer Genic enhancers | TF binding regionCpG islandChromatin interactive region | 9 gene(s) | inside rSNPs | diseases |
13 | esv1006039 | chr8:104745611-104750214 | Enhancers Weak transcription | Chromatin interactive region | n/a | inside rSNPs | diseases |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr8:104743600-104749600 | Weak transcription | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |
2 | chr8:104744000-104752000 | Weak transcription | Pancreatic Islets | Pancreatic Islet |
3 | chr8:104746400-104747800 | Weak transcription | H1 BMP4 Derived Mesendoderm Cultured Cells | ES cell derived |