Variant report
Variant | rs17641035 |
---|---|
Chromosome Location | chr2:208921257-208921258 |
allele | A/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] |
---|---|
rs10193505 | 0.94[ASN][1000 genomes] |
rs10193523 | 0.94[ASN][1000 genomes] |
rs10497894 | 0.99[ASN][1000 genomes] |
rs10804164 | 1.00[CHB][hapmap];1.00[JPT][hapmap];0.99[ASN][1000 genomes] |
rs10932220 | 0.95[CHB][hapmap];0.91[JPT][hapmap];0.89[ASN][1000 genomes] |
rs10932221 | 1.00[CHB][hapmap];0.95[JPT][hapmap];0.92[ASN][1000 genomes] |
rs10932223 | 0.99[ASN][1000 genomes] |
rs10932225 | 0.99[ASN][1000 genomes] |
rs10932226 | 0.99[ASN][1000 genomes] |
rs10932227 | 1.00[AFR][1000 genomes];0.90[AMR][1000 genomes];0.94[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs10932228 | 0.88[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.90[AMR][1000 genomes];0.94[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs11679374 | 1.00[CHB][hapmap];1.00[JPT][hapmap];0.99[ASN][1000 genomes] |
rs11687255 | 0.91[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs11688041 | 0.99[ASN][1000 genomes] |
rs11688936 | 0.96[ASN][1000 genomes] |
rs11694308 | 0.96[ASN][1000 genomes] |
rs11891423 | 0.96[ASN][1000 genomes] |
rs11893393 | 0.82[CHB][hapmap];0.91[JPT][hapmap];0.86[ASN][1000 genomes] |
rs12465154 | 0.99[ASN][1000 genomes] |
rs12469400 | 0.96[ASN][1000 genomes] |
rs12612391 | 0.95[ASN][1000 genomes] |
rs13002973 | 0.95[CHB][hapmap];0.95[JPT][hapmap];0.92[ASN][1000 genomes] |
rs13005382 | 0.95[CHB][hapmap];0.91[JPT][hapmap];0.89[ASN][1000 genomes] |
rs13018735 | 0.86[ASN][1000 genomes] |
rs13387203 | 0.94[ASN][1000 genomes] |
rs13420900 | 0.88[ASN][1000 genomes] |
rs13421034 | 0.95[CHB][hapmap];0.91[JPT][hapmap];0.88[ASN][1000 genomes] |
rs1466185 | 0.95[CHB][hapmap];0.91[JPT][hapmap];0.88[ASN][1000 genomes] |
rs1466186 | 0.88[ASN][1000 genomes] |
rs1545503 | 0.94[ASN][1000 genomes] |
rs16840362 | 0.96[ASN][1000 genomes] |
rs16840390 | 0.96[ASN][1000 genomes] |
rs16840392 | 0.96[ASN][1000 genomes] |
rs17598650 | 0.94[ASN][1000 genomes] |
rs17640827 | 0.95[CHB][hapmap];0.91[JPT][hapmap];0.88[ASN][1000 genomes] |
rs1965865 | 0.88[ASN][1000 genomes] |
rs2084870 | 0.96[ASN][1000 genomes] |
rs2084871 | 0.96[ASN][1000 genomes] |
rs2100348 | 0.96[ASN][1000 genomes] |
rs2362786 | 0.96[ASN][1000 genomes] |
rs2362788 | 0.96[ASN][1000 genomes] |
rs2362789 | 0.99[ASN][1000 genomes] |
rs2885599 | 0.96[ASN][1000 genomes] |
rs2885600 | 0.91[ASN][1000 genomes] |
rs34025579 | 0.94[ASN][1000 genomes] |
rs34335027 | 0.85[ASN][1000 genomes] |
rs34354040 | 0.96[ASN][1000 genomes] |
rs35594487 | 0.88[ASN][1000 genomes] |
rs35783183 | 0.94[ASN][1000 genomes] |
rs35968595 | 0.92[ASN][1000 genomes] |
rs4675722 | 0.96[ASN][1000 genomes] |
rs4675723 | 0.96[ASN][1000 genomes] |
rs4675724 | 0.96[ASN][1000 genomes] |
rs4675725 | 0.96[ASN][1000 genomes] |
rs4675726 | 0.96[ASN][1000 genomes] |
rs55883450 | 0.88[ASN][1000 genomes] |
rs56007263 | 0.96[ASN][1000 genomes] |
rs56340702 | 0.96[ASN][1000 genomes] |
rs56812613 | 0.85[ASN][1000 genomes] |
rs60679550 | 0.88[ASN][1000 genomes] |
rs6435403 | 0.95[ASN][1000 genomes] |
rs6435404 | 0.96[ASN][1000 genomes] |
rs6718487 | 0.96[ASN][1000 genomes] |
rs6723557 | 0.96[ASN][1000 genomes] |
rs67351199 | 0.95[ASN][1000 genomes] |
rs67417299 | 0.96[ASN][1000 genomes] |
rs6757323 | 0.96[ASN][1000 genomes] |
rs6757327 | 0.96[ASN][1000 genomes] |
rs7424035 | 0.90[ASN][1000 genomes] |
rs7559294 | 0.92[ASN][1000 genomes] |
rs7559399 | 0.92[ASN][1000 genomes] |
rs7560222 | 0.92[ASN][1000 genomes] |
rs7573629 | 0.94[ASN][1000 genomes] |
rs7582996 | 1.00[CHB][hapmap];0.95[JPT][hapmap];0.92[ASN][1000 genomes] |
rs7583013 | 1.00[CHB][hapmap];0.95[JPT][hapmap];0.92[ASN][1000 genomes] |
rs7585863 | 0.87[ASN][1000 genomes] |
rs7592525 | 0.99[ASN][1000 genomes] |
rs7599531 | 1.00[CHB][hapmap];0.95[JPT][hapmap];0.92[ASN][1000 genomes] |
rs7604044 | 0.96[ASN][1000 genomes] |
rs7608939 | 0.92[ASN][1000 genomes] |
rs7609428 | 0.92[ASN][1000 genomes] |
rs764299 | 0.94[ASN][1000 genomes] |
rs921554 | 0.94[ASN][1000 genomes] |
rs921555 | 0.94[ASN][1000 genomes] |
rs966317 | 0.96[ASN][1000 genomes] |
rs9789442 | 0.92[ASN][1000 genomes] |
rs9789446 | 1.00[CHB][hapmap];0.95[JPT][hapmap];0.92[ASN][1000 genomes] |
rs9789586 | 1.00[CHB][hapmap];0.95[JPT][hapmap];0.92[ASN][1000 genomes] |
rs9789678 | 1.00[CHB][hapmap];0.91[JPT][hapmap];0.86[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv1010531 | chr2:208610639-209176782 | Weak transcription Flanking Active TSS Enhancers Bivalent/Poised TSS Genic enhancers Active TSS Strong transcription Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNAmiRNA target site | 47 gene(s) | inside rSNPs | diseases |
2 | nsv536130 | chr2:208610639-209176782 | Weak transcription Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Active TSS Genic enhancers Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNAmiRNA target site | 47 gene(s) | inside rSNPs | diseases |
3 | nsv875743 | chr2:208688648-208940023 | Enhancers Genic enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 17 gene(s) | inside rSNPs | diseases |
4 | nsv534496 | chr2:208814372-209302791 | Strong transcription Active TSS Enhancers Weak transcription ZNF genes & repeats Genic enhancers Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 40 gene(s) | inside rSNPs | diseases |
5 | nsv961926 | chr2:208920553-208924250 | Weak transcription Bivalent Enhancer | TF binding region | 2 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr2:208912800-208929400 | Weak transcription | H1 Derived Neuronal Progenitor Cultured Cells | ES cell derived |