Variant report
Variant | rs61852610 |
---|---|
Chromosome Location | chr1:247173356-247173357 |
allele | A/G |
Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:1)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
No data |
No data |
(count:1 , 50 per page) page:
1
No. | Distal block | Cell Line | Cell type | Cell Stage |
---|---|---|---|---|
1 | chr1:247166783..247168317-chr1:247171567..247174011,2 | K562 | blood: |
No data |
No data |
No data |
No data |
rs_ID | r2[population] |
---|---|
rs10802462 | 0.90[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs10924892 | 1.00[ASN][1000 genomes] |
rs10924895 | 1.00[ASN][1000 genomes] |
rs10924896 | 1.00[ASN][1000 genomes] |
rs10924897 | 1.00[ASN][1000 genomes] |
rs10924899 | 0.85[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs1112137 | 1.00[ASN][1000 genomes] |
rs12060791 | 1.00[ASN][1000 genomes] |
rs12116484 | 0.90[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs12118487 | 1.00[ASN][1000 genomes] |
rs12120876 | 0.88[EUR][1000 genomes] |
rs12122044 | 0.85[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs12122047 | 0.82[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs12122290 | 1.00[ASN][1000 genomes] |
rs12123948 | 0.88[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs12130075 | 1.00[ASN][1000 genomes] |
rs12131419 | 1.00[ASN][1000 genomes] |
rs12135842 | 0.85[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs12135986 | 0.85[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs12139893 | 0.88[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs12141232 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs12141355 | 1.00[ASN][1000 genomes] |
rs12142305 | 0.85[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs12144260 | 1.00[ASN][1000 genomes] |
rs12563431 | 0.85[EUR][1000 genomes] |
rs1565897 | 1.00[ASN][1000 genomes] |
rs1573897 | 1.00[ASN][1000 genomes] |
rs2055191 | 1.00[ASN][1000 genomes] |
rs2055192 | 0.82[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs2172973 | 1.00[ASN][1000 genomes] |
rs2379189 | 0.91[EUR][1000 genomes] |
rs2380113 | 1.00[ASN][1000 genomes] |
rs2642957 | 0.88[EUR][1000 genomes] |
rs2642974 | 0.88[EUR][1000 genomes] |
rs2642978 | 0.88[EUR][1000 genomes] |
rs2818872 | 0.88[EUR][1000 genomes] |
rs2818874 | 0.93[EUR][1000 genomes] |
rs2818893 | 0.88[EUR][1000 genomes] |
rs28540229 | 0.90[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs28614003 | 0.97[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs41310567 | 0.83[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs4319379 | 1.00[ASN][1000 genomes] |
rs4634944 | 1.00[ASN][1000 genomes] |
rs4925540 | 1.00[ASN][1000 genomes] |
rs4925622 | 1.00[ASN][1000 genomes] |
rs4971315 | 1.00[ASN][1000 genomes] |
rs4971316 | 1.00[ASN][1000 genomes] |
rs4971317 | 1.00[ASN][1000 genomes] |
rs4971319 | 1.00[ASN][1000 genomes] |
rs55984722 | 1.00[ASN][1000 genomes] |
rs56884994 | 1.00[ASN][1000 genomes] |
rs59525684 | 1.00[ASN][1000 genomes] |
rs61373194 | 1.00[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs61498462 | 1.00[ASN][1000 genomes] |
rs61852608 | 0.90[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs61852625 | 0.83[EUR][1000 genomes] |
rs61852630 | 1.00[ASN][1000 genomes] |
rs61852637 | 1.00[ASN][1000 genomes] |
rs61852638 | 1.00[ASN][1000 genomes] |
rs61852639 | 0.90[AMR][1000 genomes];0.81[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs61852640 | 0.85[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs61852641 | 0.90[AMR][1000 genomes];0.82[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs61852642 | 1.00[ASN][1000 genomes] |
rs61852646 | 0.90[AMR][1000 genomes] |
rs6426214 | 1.00[ASN][1000 genomes] |
rs6426216 | 1.00[ASN][1000 genomes] |
rs6657686 | 1.00[ASN][1000 genomes] |
rs6664217 | 1.00[ASN][1000 genomes] |
rs6689229 | 1.00[ASN][1000 genomes] |
rs6701582 | 1.00[ASN][1000 genomes] |
rs72768397 | 1.00[ASN][1000 genomes] |
rs7418825 | 1.00[ASN][1000 genomes] |
rs7511962 | 1.00[ASN][1000 genomes] |
rs7512099 | 1.00[ASN][1000 genomes] |
rs7512150 | 1.00[ASN][1000 genomes] |
rs7513678 | 1.00[ASN][1000 genomes] |
rs7518427 | 1.00[ASN][1000 genomes] |
rs7519795 | 1.00[ASN][1000 genomes] |
rs7521422 | 0.83[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs7522300 | 1.00[ASN][1000 genomes] |
rs7526191 | 1.00[ASN][1000 genomes] |
rs7535251 | 1.00[ASN][1000 genomes] |
rs7535264 | 1.00[ASN][1000 genomes] |
rs7542852 | 1.00[ASN][1000 genomes] |
rs7543803 | 0.88[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs7546342 | 1.00[ASN][1000 genomes] |
rs7546777 | 1.00[ASN][1000 genomes] |
rs7547915 | 1.00[ASN][1000 genomes] |
rs7549105 | 1.00[ASN][1000 genomes] |
rs7549410 | 1.00[ASN][1000 genomes] |
rs7549531 | 0.81[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs7551896 | 0.83[EUR][1000 genomes];1.00[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv949571 | chr1:246688635-247240863 | Active TSS Weak transcription Flanking Active TSS Strong transcription Enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 61 gene(s) | inside rSNPs | diseases |
2 | nsv1006271 | chr1:246832606-247276182 | Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 52 gene(s) | inside rSNPs | diseases |
3 | nsv535416 | chr1:246832606-247276182 | Strong transcription ZNF genes & repeats Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 52 gene(s) | inside rSNPs | diseases |
4 | nsv873424 | chr1:246991094-247366380 | Strong transcription Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNAmiRNA target site | 42 gene(s) | inside rSNPs | diseases |
5 | nsv1005208 | chr1:247037441-247597975 | Flanking Bivalent TSS/Enh ZNF genes & repeats Active TSS Strong transcription Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNAmiRNA target site | 66 gene(s) | inside rSNPs | diseases |
6 | nsv1000602 | chr1:247044627-247226568 | Enhancers Active TSS ZNF genes & repeats Strong transcription Weak transcription Flanking Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 30 gene(s) | inside rSNPs | diseases |
7 | nsv535417 | chr1:247094131-247409000 | ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS Strong transcription Enhancers Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA | 47 gene(s) | inside rSNPs | diseases |
8 | nsv1005639 | chr1:247094161-247401380 | ZNF genes & repeats Active TSS Flanking Active TSS Weak transcription Enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA | 47 gene(s) | inside rSNPs | diseases |
9 | nsv535418 | chr1:247094161-247401380 | Active TSS ZNF genes & repeats Flanking Active TSS Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA | 47 gene(s) | inside rSNPs | diseases |
10 | nsv999879 | chr1:247112207-247276918 | Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer Enhancers Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 22 gene(s) | inside rSNPs | diseases |
11 | nsv916236 | chr1:247124353-247409065 | Weak transcription Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Flanking Active TSS Strong transcription Enhancers Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA | 36 gene(s) | inside rSNPs | diseases |
12 | nsv948419 | chr1:247130577-247400404 | ZNF genes & repeats Enhancers Transcr. at gene 5' and 3' Weak transcription Strong transcription Active TSS Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA | 35 gene(s) | inside rSNPs | diseases |
13 | nsv873427 | chr1:247140425-247218227 | ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS Enhancers Bivalent/Poised TSS Weak transcription Bivalent Enhancer Strong transcription Flanking Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 13 gene(s) | inside rSNPs | diseases |
14 | nsv549546 | chr1:247145690-247205056 | Flanking Active TSS Weak transcription ZNF genes & repeats Strong transcription Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 13 gene(s) | inside rSNPs | diseases |
15 | esv3368851 | chr1:247170017-247195360 | Active TSS Enhancers Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Weak transcription ZNF genes & repeats Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 9 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr1:247172600-247175600 | Weak transcription | HepG2 | liver |
2 | chr1:247173200-247173400 | Enhancers | Primary T killer memory cells from peripheral blood | blood |