Variant report
Variant | rs10060534 |
---|---|
Chromosome Location | chr5:111759963-111759964 |
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] |
---|---|
rs10036273 | 0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.89[ASN][1000 genomes] |
rs10036357 | 0.81[AFR][1000 genomes];0.89[ASN][1000 genomes] |
rs10039730 | 1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs10041380 | 1.00[ASN][1000 genomes] |
rs10044406 | 1.00[ASN][1000 genomes] |
rs10050630 | 0.82[ASN][1000 genomes] |
rs10051512 | 1.00[ASN][1000 genomes] |
rs10056040 | 0.81[AFR][1000 genomes];1.00[ASN][1000 genomes] |
rs10059675 | 0.85[AFR][1000 genomes];1.00[ASN][1000 genomes] |
rs10060831 | 0.82[ASN][1000 genomes] |
rs10060962 | 1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs10061025 | 1.00[ASN][1000 genomes] |
rs10061207 | 1.00[ASN][1000 genomes] |
rs10062045 | 1.00[ASN][1000 genomes] |
rs10068969 | 1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs10068974 | 1.00[ASN][1000 genomes] |
rs10069313 | 1.00[ASN][1000 genomes] |
rs10069608 | 0.81[AFR][1000 genomes];1.00[ASN][1000 genomes] |
rs10069773 | 1.00[ASN][1000 genomes] |
rs10071058 | 1.00[ASN][1000 genomes] |
rs10071862 | 0.81[AFR][1000 genomes];1.00[ASN][1000 genomes] |
rs10071986 | 0.81[AFR][1000 genomes];1.00[ASN][1000 genomes] |
rs10076627 | 1.00[ASN][1000 genomes] |
rs10077058 | 1.00[ASN][1000 genomes] |
rs10077309 | 0.81[AFR][1000 genomes];1.00[ASN][1000 genomes] |
rs10077774 | 1.00[ASN][1000 genomes] |
rs10079307 | 0.94[ASN][1000 genomes] |
rs10477480 | 0.96[AFR][1000 genomes];1.00[ASN][1000 genomes] |
rs10478086 | 1.00[ASN][1000 genomes] |
rs10515444 | 0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs10515447 | 0.87[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs12109843 | 0.87[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs12189127 | 0.94[ASN][1000 genomes] |
rs12189152 | 0.94[ASN][1000 genomes] |
rs13354202 | 0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs13354699 | 1.00[ASN][1000 genomes] |
rs13358734 | 0.80[ASN][1000 genomes] |
rs1345685 | 0.82[ASN][1000 genomes] |
rs1524423 | 1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs1524424 | 1.00[ASN][1000 genomes] |
rs17134320 | 1.00[EUR][1000 genomes] |
rs17134328 | 1.00[EUR][1000 genomes] |
rs17134339 | 1.00[EUR][1000 genomes] |
rs17134370 | 1.00[EUR][1000 genomes] |
rs17134418 | 1.00[EUR][1000 genomes] |
rs17134426 | 1.00[ASN][1000 genomes] |
rs17134429 | 1.00[ASN][1000 genomes] |
rs17134454 | 1.00[ASN][1000 genomes] |
rs17134478 | 1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs17134479 | 1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs17134502 | 0.87[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs17134556 | 1.00[EUR][1000 genomes] |
rs17134559 | 1.00[EUR][1000 genomes] |
rs17134564 | 1.00[EUR][1000 genomes] |
rs17134566 | 1.00[EUR][1000 genomes] |
rs17134569 | 1.00[EUR][1000 genomes] |
rs17134595 | 1.00[EUR][1000 genomes] |
rs17134619 | 1.00[EUR][1000 genomes] |
rs17134621 | 1.00[EUR][1000 genomes] |
rs2140624 | 1.00[EUR][1000 genomes] |
rs2416285 | 1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs28497526 | 1.00[ASN][1000 genomes] |
rs28626415 | 1.00[ASN][1000 genomes] |
rs28631626 | 0.89[ASN][1000 genomes] |
rs28716575 | 0.85[AFR][1000 genomes];1.00[ASN][1000 genomes] |
rs28806604 | 1.00[ASN][1000 genomes] |
rs28831993 | 0.96[AFR][1000 genomes];1.00[ASN][1000 genomes] |
rs28836584 | 1.00[ASN][1000 genomes] |
rs28851506 | 0.83[AFR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs28887818 | 1.00[ASN][1000 genomes] |
rs2900063 | 0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs35368801 | 1.00[EUR][1000 genomes] |
rs3903144 | 1.00[EUR][1000 genomes] |
rs3985049 | 0.83[ASN][1000 genomes] |
rs3985058 | 0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs4090543 | 1.00[EUR][1000 genomes] |
rs4441914 | 1.00[ASN][1000 genomes] |
rs57536989 | 1.00[EUR][1000 genomes] |
rs59723280 | 1.00[EUR][1000 genomes] |
rs59728660 | 0.87[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs59911735 | 1.00[EUR][1000 genomes] |
rs60901135 | 1.00[EUR][1000 genomes] |
rs6594594 | 1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs6594596 | 1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs6594597 | 0.86[AFR][1000 genomes];1.00[ASN][1000 genomes] |
rs6594599 | 0.82[ASN][1000 genomes] |
rs6860402 | 1.00[ASN][1000 genomes] |
rs6861534 | 1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs6863610 | 0.81[AFR][1000 genomes];1.00[ASN][1000 genomes] |
rs6865127 | 0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs6865907 | 1.00[EUR][1000 genomes] |
rs6866068 | 1.00[EUR][1000 genomes] |
rs6873453 | 1.00[ASN][1000 genomes] |
rs6878092 | 1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs6878158 | 0.94[ASN][1000 genomes] |
rs6879906 | 1.00[ASN][1000 genomes] |
rs6883585 | 1.00[ASN][1000 genomes] |
rs6883800 | 1.00[ASN][1000 genomes] |
rs6894395 | 0.82[ASN][1000 genomes] |
rs6895299 | 1.00[ASN][1000 genomes] |
rs721054 | 1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs721055 | 1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs73214232 | 1.00[EUR][1000 genomes] |
rs73214236 | 1.00[EUR][1000 genomes] |
rs73214243 | 1.00[EUR][1000 genomes] |
rs73214250 | 1.00[EUR][1000 genomes] |
rs73214252 | 1.00[EUR][1000 genomes] |
rs73214254 | 1.00[ASN][1000 genomes] |
rs73214255 | 1.00[EUR][1000 genomes] |
rs73214256 | 1.00[ASN][1000 genomes] |
rs73214261 | 1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs73214264 | 1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs73214269 | 1.00[EUR][1000 genomes] |
rs73214270 | 1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs73214272 | 1.00[ASN][1000 genomes] |
rs73214274 | 1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs73216591 | 1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs73216602 | 1.00[EUR][1000 genomes] |
rs73218303 | 1.00[EUR][1000 genomes] |
rs73218309 | 1.00[EUR][1000 genomes] |
rs73218315 | 1.00[EUR][1000 genomes] |
rs73218319 | 1.00[EUR][1000 genomes] |
rs73218321 | 1.00[ASN][1000 genomes] |
rs73218324 | 0.87[AMR][1000 genomes] |
rs73218335 | 1.00[EUR][1000 genomes] |
rs73218338 | 0.94[ASN][1000 genomes] |
rs73218339 | 0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs73218340 | 0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs73218343 | 0.83[AFR][1000 genomes];1.00[ASN][1000 genomes] |
rs73218345 | 1.00[EUR][1000 genomes] |
rs73218347 | 0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs73218348 | 0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs73218349 | 0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs73220307 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs73220310 | 1.00[EUR][1000 genomes] |
rs73220313 | 1.00[EUR][1000 genomes] |
rs73222143 | 1.00[EUR][1000 genomes] |
rs73222145 | 1.00[EUR][1000 genomes] |
rs73222146 | 1.00[EUR][1000 genomes] |
rs73222148 | 1.00[EUR][1000 genomes] |
rs73222150 | 1.00[EUR][1000 genomes] |
rs73222155 | 1.00[EUR][1000 genomes] |
rs73222163 | 1.00[EUR][1000 genomes] |
rs73222167 | 1.00[EUR][1000 genomes] |
rs7446816 | 1.00[EUR][1000 genomes] |
rs7702830 | 0.94[ASN][1000 genomes] |
rs7702999 | 1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs7705094 | 1.00[ASN][1000 genomes] |
rs7706551 | 1.00[ASN][1000 genomes] |
rs7706737 | 1.00[ASN][1000 genomes] |
rs7707028 | 1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs7709879 | 0.84[AFR][1000 genomes];1.00[ASN][1000 genomes] |
rs7709963 | 0.84[AFR][1000 genomes];1.00[ASN][1000 genomes] |
rs7710041 | 0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs7710063 | 1.00[ASN][1000 genomes] |
rs7710507 | 1.00[ASN][1000 genomes] |
rs7711662 | 0.81[AFR][1000 genomes];1.00[ASN][1000 genomes] |
rs7714450 | 1.00[ASN][1000 genomes] |
rs7725728 | 1.00[ASN][1000 genomes] |
rs7725742 | 1.00[ASN][1000 genomes] |
rs7730739 | 1.00[ASN][1000 genomes] |
rs7733415 | 1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs7736305 | 1.00[ASN][1000 genomes] |
rs7736457 | 0.82[ASN][1000 genomes] |
rs821737 | 1.00[EUR][1000 genomes] |
rs821740 | 1.00[EUR][1000 genomes] |
rs821741 | 1.00[EUR][1000 genomes] |
rs821742 | 1.00[EUR][1000 genomes] |
rs821743 | 1.00[EUR][1000 genomes] |
rs866597 | 1.00[EUR][1000 genomes] |
rs9326853 | 0.94[ASN][1000 genomes] |
rs956273 | 1.00[EUR][1000 genomes] |
rs9654518 | 1.00[ASN][1000 genomes] |
rs985873 | 1.00[ASN][1000 genomes] |
rs986797 | 1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs9885182 | 1.00[ASN][1000 genomes] |
rs9885209 | 1.00[ASN][1000 genomes] |
rs9885211 | 1.00[ASN][1000 genomes] |
rs9885390 | 1.00[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv1015302 | chr5:111339022-111802947 | Enhancers Active TSS Strong transcription Weak transcription Bivalent/Poised TSS Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 26 gene(s) | inside rSNPs | diseases |
2 | nsv537861 | chr5:111339022-111802947 | Strong transcription Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 26 gene(s) | inside rSNPs | diseases |
3 | nsv599368 | chr5:111399885-112032675 | Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Genic enhancers Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 35 gene(s) | inside rSNPs | diseases |
4 | nsv882714 | chr5:111655382-111807579 | Enhancers Flanking Active TSS Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Genic enhancers Bivalent Enhancer Strong transcription ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNA | 6 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr5:111756600-111767200 | Weak transcription | Pancreatic Islets | Pancreatic Islet |
2 | chr5:111759800-111760000 | Enhancers | H1 Cell Line | embryonic stem cell |
3 | chr5:111759800-111760000 | Enhancers | HUES6 Cell Line | embryonic stem cell |