Variant report
Variant | rs34605921 |
---|---|
Chromosome Location | chr1:169143794-169143795 |
allele | C/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] |
---|---|
rs10800403 | 0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.90[ASN][1000 genomes] |
rs10800406 | 0.93[ASN][1000 genomes] |
rs10800407 | 0.93[ASN][1000 genomes] |
rs10800410 | 0.91[ASN][1000 genomes] |
rs10800411 | 0.91[ASN][1000 genomes] |
rs1080267 | 0.89[EUR][1000 genomes] |
rs10919073 | 0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs10919076 | 0.93[ASN][1000 genomes] |
rs10919082 | 1.00[ASN][1000 genomes] |
rs10919083 | 1.00[ASN][1000 genomes] |
rs10919084 | 1.00[ASN][1000 genomes] |
rs10919086 | 1.00[ASN][1000 genomes] |
rs10919090 | 0.91[ASN][1000 genomes] |
rs10919094 | 0.91[ASN][1000 genomes] |
rs1138486 | 0.91[AMR][1000 genomes];0.98[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs11801853 | 0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs11802117 | 1.00[ASN][1000 genomes] |
rs11809180 | 0.91[AMR][1000 genomes];0.98[EUR][1000 genomes];0.90[ASN][1000 genomes] |
rs12057856 | 1.00[ASN][1000 genomes] |
rs12065884 | 1.00[ASN][1000 genomes] |
rs12066676 | 0.90[AMR][1000 genomes];0.92[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs12067018 | 1.00[ASN][1000 genomes] |
rs12067072 | 0.93[ASN][1000 genomes] |
rs12070626 | 0.90[AMR][1000 genomes];0.92[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs12071277 | 0.93[ASN][1000 genomes] |
rs12072226 | 1.00[ASN][1000 genomes] |
rs12072953 | 1.00[ASN][1000 genomes] |
rs12075832 | 0.93[ASN][1000 genomes] |
rs12076469 | 0.99[ASN][1000 genomes] |
rs12076510 | 0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs12079745 | 0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.90[ASN][1000 genomes] |
rs12082618 | 0.93[ASN][1000 genomes] |
rs12082810 | 0.93[ASN][1000 genomes] |
rs12083287 | 0.82[ASN][1000 genomes] |
rs12084964 | 0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs12086104 | 0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs12086292 | 0.93[ASN][1000 genomes] |
rs12086983 | 0.93[ASN][1000 genomes] |
rs12089118 | 0.93[ASN][1000 genomes] |
rs12095171 | 0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs12120493 | 1.00[ASN][1000 genomes] |
rs12124144 | 1.00[ASN][1000 genomes] |
rs12124168 | 1.00[ASN][1000 genomes] |
rs12124744 | 0.92[ASN][1000 genomes] |
rs12125921 | 1.00[ASN][1000 genomes] |
rs12125985 | 1.00[ASN][1000 genomes] |
rs12126032 | 0.93[ASN][1000 genomes] |
rs12127305 | 0.93[ASN][1000 genomes] |
rs12127613 | 0.98[ASN][1000 genomes] |
rs12129969 | 0.91[ASN][1000 genomes] |
rs12129979 | 0.89[ASN][1000 genomes] |
rs12130764 | 0.91[ASN][1000 genomes] |
rs12135928 | 0.93[ASN][1000 genomes] |
rs12140967 | 0.93[ASN][1000 genomes] |
rs12143131 | 0.93[ASN][1000 genomes] |
rs12143135 | 0.81[ASN][1000 genomes] |
rs12143965 | 0.99[ASN][1000 genomes] |
rs12144705 | 0.96[ASN][1000 genomes] |
rs12145939 | 0.93[ASN][1000 genomes] |
rs12354315 | 0.93[ASN][1000 genomes] |
rs12562404 | 1.00[ASN][1000 genomes] |
rs12564558 | 0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs12564596 | 1.00[ASN][1000 genomes] |
rs12568636 | 0.91[ASN][1000 genomes] |
rs12724812 | 1.00[ASN][1000 genomes] |
rs12724863 | 0.91[ASN][1000 genomes] |
rs12734206 | 0.91[ASN][1000 genomes] |
rs12735503 | 1.00[ASN][1000 genomes] |
rs12736110 | 1.00[ASN][1000 genomes] |
rs12736723 | 0.91[ASN][1000 genomes] |
rs12744184 | 1.00[ASN][1000 genomes] |
rs12744341 | 1.00[ASN][1000 genomes] |
rs12744655 | 0.96[ASN][1000 genomes] |
rs12745732 | 0.80[ASN][1000 genomes] |
rs12747242 | 0.93[ASN][1000 genomes] |
rs12755385 | 1.00[ASN][1000 genomes] |
rs12756799 | 1.00[ASN][1000 genomes] |
rs12758208 | 0.93[ASN][1000 genomes] |
rs1320965 | 0.93[ASN][1000 genomes] |
rs1320966 | 0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs1320967 | 0.93[ASN][1000 genomes] |
rs1320968 | 0.93[ASN][1000 genomes] |
rs1358712 | 0.93[ASN][1000 genomes] |
rs1419323 | 0.93[ASN][1000 genomes] |
rs1419324 | 0.93[ASN][1000 genomes] |
rs1830492 | 0.89[ASN][1000 genomes] |
rs1830493 | 0.85[ASN][1000 genomes] |
rs1830494 | 0.90[ASN][1000 genomes] |
rs1830495 | 0.99[ASN][1000 genomes] |
rs2032044 | 0.93[ASN][1000 genomes] |
rs2050119 | 1.00[ASN][1000 genomes] |
rs2143287 | 0.93[ASN][1000 genomes] |
rs2179492 | 0.91[ASN][1000 genomes] |
rs2420010 | 0.90[ASN][1000 genomes] |
rs34250651 | 1.00[ASN][1000 genomes] |
rs34645703 | 0.88[AMR][1000 genomes];0.98[EUR][1000 genomes];0.82[ASN][1000 genomes] |
rs34847919 | 0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs35037551 | 0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs35631014 | 1.00[ASN][1000 genomes] |
rs35774511 | 1.00[ASN][1000 genomes] |
rs3737681 | 1.00[ASN][1000 genomes] |
rs3766045 | 0.90[AMR][1000 genomes];0.92[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs3766053 | 0.93[ASN][1000 genomes] |
rs3766054 | 0.93[ASN][1000 genomes] |
rs3766055 | 0.93[ASN][1000 genomes] |
rs3766059 | 1.00[ASN][1000 genomes] |
rs3766060 | 1.00[ASN][1000 genomes] |
rs3766061 | 0.86[ASN][1000 genomes] |
rs3766062 | 0.93[ASN][1000 genomes] |
rs3766063 | 0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs3766065 | 0.91[ASN][1000 genomes] |
rs3766066 | 0.91[ASN][1000 genomes] |
rs3766067 | 0.91[ASN][1000 genomes] |
rs3766069 | 0.91[ASN][1000 genomes] |
rs3766070 | 0.91[ASN][1000 genomes] |
rs3766071 | 0.91[ASN][1000 genomes] |
rs3820053 | 1.00[ASN][1000 genomes] |
rs3820055 | 0.99[ASN][1000 genomes] |
rs3820056 | 0.99[ASN][1000 genomes] |
rs4140540 | 0.91[ASN][1000 genomes] |
rs4656653 | 0.93[ASN][1000 genomes] |
rs4656654 | 1.00[ASN][1000 genomes] |
rs4656655 | 1.00[ASN][1000 genomes] |
rs4656656 | 1.00[ASN][1000 genomes] |
rs4656659 | 0.93[ASN][1000 genomes] |
rs4656660 | 0.89[ASN][1000 genomes] |
rs61806209 | 0.97[ASN][1000 genomes] |
rs6695177 | 1.00[ASN][1000 genomes] |
rs6695252 | 1.00[ASN][1000 genomes] |
rs67485965 | 1.00[ASN][1000 genomes] |
rs72637225 | 0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs745922 | 0.93[ASN][1000 genomes] |
rs7518554 | 1.00[ASN][1000 genomes] |
rs7526721 | 0.81[ASN][1000 genomes] |
rs7529937 | 0.90[ASN][1000 genomes] |
rs7541564 | 1.00[ASN][1000 genomes] |
rs7541675 | 1.00[ASN][1000 genomes] |
rs7541700 | 1.00[ASN][1000 genomes] |
rs7552484 | 0.93[ASN][1000 genomes] |
rs909929 | 0.90[ASN][1000 genomes] |
rs909930 | 0.91[ASN][1000 genomes] |
rs909931 | 0.91[ASN][1000 genomes] |
rs932394 | 1.00[ASN][1000 genomes] |
rs932395 | 1.00[ASN][1000 genomes] |
rs958581 | 1.00[ASN][1000 genomes] |
rs9887854 | 0.93[ASN][1000 genomes] |
rs9887857 | 0.93[ASN][1000 genomes] |
rs9887903 | 0.93[ASN][1000 genomes] |
rs9887916 | 0.91[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv869415 | chr1:168467284-169153863 | Flanking Active TSS Weak transcription Enhancers Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Genic enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNA | 44 gene(s) | inside rSNPs | diseases |
2 | esv3522071 | chr1:168978325-169339044 | Weak transcription Enhancers Flanking Active TSS Strong transcription Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 35 gene(s) | inside rSNPs | diseases |
3 | esv3522072 | chr1:168978325-169339044 | Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Strong transcription Transcr. at gene 5' and 3' Weak transcription Genic enhancers ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 35 gene(s) | inside rSNPs | diseases |
4 | nsv831858 | chr1:169022383-169179068 | Weak transcription Flanking Active TSS Active TSS Strong transcription Enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNA | 29 gene(s) | inside rSNPs | diseases |
5 | esv10418 | chr1:169059628-169621268 | Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers Strong transcription ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 56 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr1:169130400-169195200 | Weak transcription | Pancreas | Pancrea |
2 | chr1:169131400-169149400 | Weak transcription | Foreskin Keratinocyte Primary Cells skin02 | Skin |
3 | chr1:169137600-169158000 | Weak transcription | Primary T cells from cord blood | blood |
4 | chr1:169139000-169147000 | Weak transcription | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |