Variant report
Variant | rs7016124 |
---|---|
Chromosome Location | chr8:52236558-52236559 |
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] |
---|---|
rs1003095 | 0.81[EUR][1000 genomes] |
rs10091279 | 0.88[JPT][hapmap];0.81[EUR][1000 genomes] |
rs10092020 | 0.81[EUR][1000 genomes] |
rs10094879 | 0.94[EUR][1000 genomes] |
rs10097749 | 0.94[EUR][1000 genomes] |
rs10101803 | 0.81[EUR][1000 genomes] |
rs10102454 | 0.96[EUR][1000 genomes] |
rs10105228 | 0.98[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs10107148 | 0.94[EUR][1000 genomes] |
rs10110193 | 0.98[EUR][1000 genomes] |
rs10113485 | 0.94[EUR][1000 genomes] |
rs1017352 | 0.88[JPT][hapmap] |
rs1017353 | 0.88[JPT][hapmap] |
rs1017354 | 0.88[JPT][hapmap] |
rs1052704 | 1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs10958261 | 0.88[JPT][hapmap];0.83[EUR][1000 genomes] |
rs11989863 | 0.94[EUR][1000 genomes] |
rs11991037 | 0.98[EUR][1000 genomes] |
rs11993179 | 0.83[EUR][1000 genomes] |
rs1219677 | 0.88[JPT][hapmap];0.81[EUR][1000 genomes] |
rs1219680 | 0.86[JPT][hapmap];0.81[EUR][1000 genomes] |
rs1236097 | 0.88[JPT][hapmap] |
rs12542121 | 0.96[EUR][1000 genomes] |
rs12550267 | 0.86[JPT][hapmap];0.83[EUR][1000 genomes] |
rs1346954 | 0.86[JPT][hapmap] |
rs1370446 | 0.88[JPT][hapmap];0.92[AFR][1000 genomes];0.90[AMR][1000 genomes];0.99[EUR][1000 genomes] |
rs1431619 | 0.86[JPT][hapmap] |
rs1431620 | 0.88[JPT][hapmap] |
rs1431624 | 0.86[JPT][hapmap] |
rs1431625 | 0.88[JPT][hapmap] |
rs1431626 | 0.88[JPT][hapmap] |
rs1431627 | 0.88[JPT][hapmap] |
rs1431628 | 0.88[JPT][hapmap] |
rs1560508 | 0.88[JPT][hapmap] |
rs1560509 | 0.88[JPT][hapmap] |
rs1560510 | 0.86[JPT][hapmap] |
rs16915954 | 0.94[EUR][1000 genomes] |
rs16915972 | 0.94[EUR][1000 genomes] |
rs16916011 | 0.80[EUR][1000 genomes] |
rs17261657 | 0.88[JPT][hapmap] |
rs1816630 | 1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs1837086 | 0.98[EUR][1000 genomes] |
rs1837087 | 0.98[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs1991691 | 0.88[JPT][hapmap] |
rs1991692 | 0.88[JPT][hapmap] |
rs2217988 | 1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[AFR][1000 genomes];0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs28417640 | 0.98[EUR][1000 genomes] |
rs28449829 | 0.98[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs28522270 | 0.81[AMR][1000 genomes];0.80[EUR][1000 genomes] |
rs28534083 | 0.98[EUR][1000 genomes] |
rs28805429 | 0.81[AFR][1000 genomes];0.87[AMR][1000 genomes];0.84[EUR][1000 genomes] |
rs2915454 | 0.88[JPT][hapmap] |
rs2915457 | 0.88[JPT][hapmap] |
rs2915460 | 0.88[JPT][hapmap] |
rs2915461 | 0.88[JPT][hapmap] |
rs2915465 | 0.86[JPT][hapmap] |
rs2915467 | 0.86[JPT][hapmap] |
rs2915468 | 0.88[JPT][hapmap] |
rs2915469 | 0.88[JPT][hapmap] |
rs2915471 | 0.88[JPT][hapmap] |
rs2915473 | 0.88[JPT][hapmap] |
rs2915475 | 0.86[JPT][hapmap] |
rs2915476 | 0.88[JPT][hapmap] |
rs2915477 | 0.88[JPT][hapmap] |
rs2915479 | 0.86[JPT][hapmap] |
rs2915480 | 0.88[JPT][hapmap] |
rs2915481 | 0.88[JPT][hapmap] |
rs2915482 | 0.88[JPT][hapmap] |
rs2915483 | 0.88[JPT][hapmap] |
rs2915485 | 0.88[JPT][hapmap] |
rs2976984 | 0.86[JPT][hapmap] |
rs2976985 | 0.88[JPT][hapmap] |
rs2976986 | 0.88[JPT][hapmap] |
rs2976988 | 0.88[JPT][hapmap] |
rs2976989 | 0.86[JPT][hapmap] |
rs2976990 | 0.88[JPT][hapmap] |
rs2976992 | 0.88[JPT][hapmap] |
rs2976993 | 0.88[JPT][hapmap] |
rs2976994 | 0.86[JPT][hapmap] |
rs3097703 | 0.88[JPT][hapmap] |
rs3097704 | 0.88[JPT][hapmap] |
rs3097705 | 0.88[JPT][hapmap] |
rs3097706 | 0.88[JPT][hapmap] |
rs3115784 | 0.88[JPT][hapmap] |
rs4471026 | 0.83[EUR][1000 genomes];0.90[ASN][1000 genomes] |
rs4500070 | 0.82[EUR][1000 genomes] |
rs4873192 | 0.98[EUR][1000 genomes] |
rs4873533 | 0.93[EUR][1000 genomes] |
rs4873534 | 0.94[EUR][1000 genomes] |
rs4873540 | 0.98[EUR][1000 genomes] |
rs4873541 | 0.81[EUR][1000 genomes] |
rs4873542 | 0.98[EUR][1000 genomes] |
rs4873543 | 0.90[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs4873544 | 0.92[AFR][1000 genomes];0.90[AMR][1000 genomes];0.99[EUR][1000 genomes] |
rs4873545 | 0.81[EUR][1000 genomes] |
rs60579236 | 0.83[EUR][1000 genomes] |
rs60646659 | 0.81[EUR][1000 genomes] |
rs6473594 | 0.81[EUR][1000 genomes] |
rs6473595 | 0.98[EUR][1000 genomes] |
rs66555193 | 0.98[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs67110071 | 0.83[EUR][1000 genomes] |
rs67134977 | 0.81[EUR][1000 genomes] |
rs67152383 | 0.83[EUR][1000 genomes] |
rs6981422 | 0.81[EUR][1000 genomes] |
rs6986651 | 0.98[EUR][1000 genomes] |
rs6987616 | 0.97[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs6987775 | 0.91[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs6992933 | 0.93[EUR][1000 genomes] |
rs6996951 | 0.81[EUR][1000 genomes] |
rs6998723 | 0.96[EUR][1000 genomes] |
rs6998855 | 1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs6999446 | 0.98[EUR][1000 genomes] |
rs7000176 | 0.81[EUR][1000 genomes] |
rs7003720 | 0.83[EUR][1000 genomes] |
rs7004460 | 0.81[EUR][1000 genomes] |
rs7008365 | 0.93[EUR][1000 genomes] |
rs7016775 | 0.82[JPT][hapmap];0.83[AFR][1000 genomes];0.88[AMR][1000 genomes];0.85[EUR][1000 genomes] |
rs7017403 | 1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs7017421 | 1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs726127 | 0.81[EUR][1000 genomes] |
rs766788 | 0.81[EUR][1000 genomes] |
rs766789 | 0.81[EUR][1000 genomes] |
rs766790 | 0.81[EUR][1000 genomes] |
rs7813377 | 0.82[EUR][1000 genomes] |
rs7814566 | 0.96[AFR][1000 genomes];0.90[AMR][1000 genomes];0.99[EUR][1000 genomes] |
rs7818411 | 0.83[AMR][1000 genomes];0.83[EUR][1000 genomes] |
rs7818590 | 0.97[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs7818710 | 0.96[EUR][1000 genomes] |
rs7821565 | 0.96[EUR][1000 genomes] |
rs7825017 | 0.94[EUR][1000 genomes] |
rs7827306 | 0.88[JPT][hapmap];0.96[AFR][1000 genomes];0.90[AMR][1000 genomes];0.99[EUR][1000 genomes] |
rs7827446 | 0.88[JPT][hapmap];0.96[AFR][1000 genomes];0.90[AMR][1000 genomes];0.99[EUR][1000 genomes] |
rs7828080 | 0.81[EUR][1000 genomes] |
rs7834299 | 0.81[EUR][1000 genomes] |
rs7839630 | 0.97[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs7842457 | 0.98[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs7844531 | 0.96[EUR][1000 genomes] |
rs7844947 | 0.93[EUR][1000 genomes] |
rs7845311 | 0.82[EUR][1000 genomes] |
rs7846115 | 0.81[EUR][1000 genomes] |
rs9298442 | 0.98[EUR][1000 genomes] |
rs9298443 | 0.81[EUR][1000 genomes] |
rs9298444 | 0.81[EUR][1000 genomes] |
rs972025 | 0.86[JPT][hapmap] |
rs972026 | 0.86[JPT][hapmap];0.80[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv932026 | chr8:51858658-52758574 | Strong transcription Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Active TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 10 gene(s) | inside rSNPs | diseases |
2 | nsv948338 | chr8:52060314-52368754 | Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 4 gene(s) | inside rSNPs | diseases |
3 | nsv890895 | chr8:52190571-52615191 | Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 4 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr8:52221200-52238000 | Weak transcription | Left Ventricle | heart |