Variant report
Variant | rs66760984 |
---|---|
Chromosome Location | chr19:21824706-21824707 |
allele | A/C |
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] |
---|---|
rs10153511 | 0.91[AFR][1000 genomes];0.87[AMR][1000 genomes];0.86[EUR][1000 genomes];0.87[ASN][1000 genomes] |
rs10153514 | 0.90[AFR][1000 genomes];0.87[AMR][1000 genomes];0.83[EUR][1000 genomes];0.87[ASN][1000 genomes] |
rs10401456 | 0.83[AFR][1000 genomes] |
rs10404030 | 0.83[AFR][1000 genomes] |
rs10405733 | 0.83[AFR][1000 genomes] |
rs10418334 | 0.92[AFR][1000 genomes];0.91[AMR][1000 genomes];0.88[EUR][1000 genomes];0.85[ASN][1000 genomes] |
rs10422946 | 0.83[AFR][1000 genomes] |
rs11883213 | 0.91[AFR][1000 genomes];0.88[AMR][1000 genomes];0.87[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs12232878 | 0.81[AFR][1000 genomes];0.89[AMR][1000 genomes];0.83[ASN][1000 genomes] |
rs12232880 | 0.83[AFR][1000 genomes];0.89[AMR][1000 genomes];0.81[EUR][1000 genomes];0.83[ASN][1000 genomes] |
rs12232882 | 0.80[AFR][1000 genomes];0.88[AMR][1000 genomes] |
rs12972465 | 0.82[AFR][1000 genomes] |
rs12972876 | 0.81[AFR][1000 genomes] |
rs12972948 | 0.83[AFR][1000 genomes] |
rs12973438 | 0.83[AFR][1000 genomes] |
rs12974037 | 0.83[AFR][1000 genomes] |
rs12983182 | 0.83[AFR][1000 genomes] |
rs12983603 | 0.86[AFR][1000 genomes] |
rs12983724 | 0.83[AFR][1000 genomes] |
rs12984244 | 0.83[AFR][1000 genomes] |
rs12984552 | 0.83[AFR][1000 genomes] |
rs12985310 | 0.85[AFR][1000 genomes] |
rs1520074 | 0.83[AFR][1000 genomes] |
rs2359408 | 0.82[AFR][1000 genomes] |
rs2359409 | 0.83[AFR][1000 genomes] |
rs2884702 | 0.80[AMR][1000 genomes] |
rs34030908 | 0.83[AFR][1000 genomes];0.84[AMR][1000 genomes];0.80[ASN][1000 genomes] |
rs34063774 | 0.83[AFR][1000 genomes];0.88[AMR][1000 genomes];0.83[ASN][1000 genomes] |
rs34186261 | 0.83[AFR][1000 genomes];0.88[AMR][1000 genomes];0.83[ASN][1000 genomes] |
rs34191116 | 0.84[AFR][1000 genomes];0.80[AMR][1000 genomes] |
rs34296298 | 0.84[AFR][1000 genomes] |
rs34391950 | 0.84[AFR][1000 genomes] |
rs34414071 | 0.85[AFR][1000 genomes] |
rs34465727 | 0.84[AFR][1000 genomes] |
rs34489089 | 0.83[AFR][1000 genomes];0.88[AMR][1000 genomes];0.80[EUR][1000 genomes];0.82[ASN][1000 genomes] |
rs34505911 | 0.84[AFR][1000 genomes] |
rs34702084 | 0.85[AFR][1000 genomes];0.80[AMR][1000 genomes] |
rs34729710 | 0.84[AFR][1000 genomes];0.80[AMR][1000 genomes] |
rs34787886 | 0.81[AMR][1000 genomes] |
rs34810593 | 0.84[AFR][1000 genomes];0.91[AMR][1000 genomes];0.82[EUR][1000 genomes];0.84[ASN][1000 genomes] |
rs34943457 | 0.87[AFR][1000 genomes];0.89[AMR][1000 genomes];0.81[EUR][1000 genomes];0.84[ASN][1000 genomes] |
rs35007061 | 0.85[AFR][1000 genomes];0.80[AMR][1000 genomes] |
rs35063624 | 0.83[AFR][1000 genomes];0.88[AMR][1000 genomes];0.80[EUR][1000 genomes];0.82[ASN][1000 genomes] |
rs35079667 | 0.84[AFR][1000 genomes] |
rs35079912 | 0.83[AFR][1000 genomes];0.85[AMR][1000 genomes] |
rs35134927 | 0.83[AFR][1000 genomes];0.88[AMR][1000 genomes];0.80[EUR][1000 genomes];0.82[ASN][1000 genomes] |
rs35211334 | 0.83[AFR][1000 genomes];0.87[AMR][1000 genomes];0.80[EUR][1000 genomes] |
rs35221615 | 0.85[AFR][1000 genomes] |
rs35257760 | 0.84[AFR][1000 genomes] |
rs35279419 | 0.83[AFR][1000 genomes];0.83[AMR][1000 genomes] |
rs35397389 | 0.81[AFR][1000 genomes] |
rs35586674 | 0.84[AMR][1000 genomes] |
rs35733534 | 0.83[AFR][1000 genomes];0.85[AMR][1000 genomes];0.80[EUR][1000 genomes] |
rs35947380 | 0.83[AFR][1000 genomes];0.88[AMR][1000 genomes];0.81[ASN][1000 genomes] |
rs35970173 | 0.83[AFR][1000 genomes];0.87[AMR][1000 genomes] |
rs36031236 | 0.81[AFR][1000 genomes];0.84[AMR][1000 genomes] |
rs36094732 | 0.84[AFR][1000 genomes] |
rs36150731 | 0.81[AFR][1000 genomes] |
rs36184440 | 0.87[AFR][1000 genomes];0.89[AMR][1000 genomes];0.82[EUR][1000 genomes];0.84[ASN][1000 genomes] |
rs36186361 | 0.82[AFR][1000 genomes] |
rs4808287 | 0.83[AFR][1000 genomes] |
rs4808289 | 0.83[AFR][1000 genomes] |
rs4809170 | 0.83[AFR][1000 genomes] |
rs55804010 | 0.87[AFR][1000 genomes];0.89[AMR][1000 genomes];0.81[EUR][1000 genomes];0.84[ASN][1000 genomes] |
rs62108442 | 0.88[AFR][1000 genomes];0.91[AMR][1000 genomes];0.84[EUR][1000 genomes];0.84[ASN][1000 genomes] |
rs62108444 | 0.90[AFR][1000 genomes];0.89[AMR][1000 genomes];0.82[EUR][1000 genomes];0.84[ASN][1000 genomes] |
rs62108456 | 0.81[AFR][1000 genomes] |
rs62109860 | 0.85[AFR][1000 genomes] |
rs62109861 | 0.85[AFR][1000 genomes] |
rs6511279 | 0.83[AFR][1000 genomes] |
rs6511280 | 0.83[AFR][1000 genomes] |
rs6511281 | 0.83[AFR][1000 genomes] |
rs66519141 | 0.83[AFR][1000 genomes] |
rs66536336 | 0.83[AFR][1000 genomes] |
rs66562280 | 0.82[AFR][1000 genomes] |
rs66628182 | 0.97[AFR][1000 genomes];0.99[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs66740503 | 0.95[AFR][1000 genomes];0.97[AMR][1000 genomes];0.94[EUR][1000 genomes];0.95[ASN][1000 genomes] |
rs66790650 | 0.84[AFR][1000 genomes] |
rs66846030 | 0.83[AFR][1000 genomes] |
rs66876878 | 0.82[AFR][1000 genomes] |
rs66952332 | 0.84[AMR][1000 genomes];0.80[ASN][1000 genomes] |
rs67042975 | 0.81[AFR][1000 genomes] |
rs67057011 | 0.83[AMR][1000 genomes];0.80[ASN][1000 genomes] |
rs67351081 | 0.85[AFR][1000 genomes] |
rs67395636 | 0.91[AFR][1000 genomes];0.95[AMR][1000 genomes];0.90[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs67487679 | 0.84[AFR][1000 genomes] |
rs67488540 | 0.84[AMR][1000 genomes] |
rs67542605 | 0.83[AFR][1000 genomes];0.84[AMR][1000 genomes] |
rs68026986 | 0.83[AFR][1000 genomes];0.83[AMR][1000 genomes] |
rs68089169 | 0.92[AFR][1000 genomes];0.93[AMR][1000 genomes];0.89[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs68132044 | 0.83[AMR][1000 genomes];0.80[ASN][1000 genomes] |
rs68187621 | 0.82[AFR][1000 genomes] |
rs71333835 | 0.80[AFR][1000 genomes];0.92[AMR][1000 genomes];0.87[EUR][1000 genomes];0.90[ASN][1000 genomes] |
rs71333836 | 0.83[AFR][1000 genomes];0.95[AMR][1000 genomes];0.87[EUR][1000 genomes];0.92[ASN][1000 genomes] |
rs71333837 | 0.85[AFR][1000 genomes];0.95[AMR][1000 genomes];0.88[EUR][1000 genomes];0.92[ASN][1000 genomes] |
rs71333840 | 0.82[AFR][1000 genomes] |
rs71333841 | 0.84[AFR][1000 genomes] |
rs71333850 | 0.85[AFR][1000 genomes] |
rs8103003 | 0.83[AFR][1000 genomes];0.87[AMR][1000 genomes];0.80[EUR][1000 genomes] |
rs8103014 | 0.80[AFR][1000 genomes] |
rs8103174 | 0.83[AFR][1000 genomes];0.81[AMR][1000 genomes] |
rs8103271 | 0.83[AFR][1000 genomes];0.85[AMR][1000 genomes];0.80[ASN][1000 genomes] |
rs8104224 | 0.81[AFR][1000 genomes];0.84[AMR][1000 genomes] |
rs8106449 | 0.83[AFR][1000 genomes] |
rs9304989 | 0.87[AFR][1000 genomes];0.87[AMR][1000 genomes];0.86[EUR][1000 genomes];0.82[ASN][1000 genomes] |
rs9676455 | 0.84[AFR][1000 genomes];0.87[AMR][1000 genomes] |
rs9676469 | 0.85[AMR][1000 genomes] |
rs9676508 | 0.82[AMR][1000 genomes] |
rs9807876 | 0.83[AFR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | esv3414204 | chr19:21301761-21839451 | ZNF genes & repeats Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Strong transcription Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Genic enhancers Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 44 gene(s) | inside rSNPs | diseases |
2 | nsv578952 | chr19:21535707-21868584 | Genic enhancers Active TSS ZNF genes & repeats Enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 34 gene(s) | inside rSNPs | diseases |
3 | nsv833782 | chr19:21663537-21845722 | Weak transcription Enhancers Active TSS ZNF genes & repeats Strong transcription Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 23 gene(s) | inside rSNPs | diseases |
4 | nsv911422 | chr19:21752009-21973929 | ZNF genes & repeats Strong transcription Active TSS Genic enhancers Weak transcription Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 13 gene(s) | inside rSNPs | diseases |
5 | esv3441368 | chr19:21781459-22182822 | Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Enhancers Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 18 gene(s) | inside rSNPs | diseases |
6 | esv3339694 | chr19:21781479-22182792 | Enhancers Active TSS ZNF genes & repeats Weak transcription Bivalent/Poised TSS Flanking Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 18 gene(s) | inside rSNPs | diseases |
7 | nsv1063115 | chr19:21782104-22528039 | Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 38 gene(s) | inside rSNPs | diseases |
8 | nsv911423 | chr19:21783995-21858994 | Weak transcription Enhancers Flanking Active TSS Strong transcription Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 3 gene(s) | inside rSNPs | diseases |
9 | nsv458525 | chr19:21796943-22019697 | Weak transcription ZNF genes & repeats Active TSS Strong transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 13 gene(s) | inside rSNPs | diseases |
10 | nsv578969 | chr19:21796943-22019697 | ZNF genes & repeats Active TSS Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 13 gene(s) | inside rSNPs | diseases |
11 | esv3392559 | chr19:21798396-21965956 | Weak transcription Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS Enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 10 gene(s) | inside rSNPs | diseases |
12 | esv2760530 | chr19:21798427-21885936 | Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 4 gene(s) | inside rSNPs | diseases |
13 | nsv911424 | chr19:21798441-22471156 | Strong transcription Enhancers Active TSS ZNF genes & repeats Weak transcription Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 36 gene(s) | inside rSNPs | diseases |
14 | nsv963135 | chr19:21800743-21892052 | Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 5 gene(s) | inside rSNPs | diseases |
15 | nsv138061 | chr19:21818959-21828721 | Weak transcription | TF binding regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
16 | nsv978790 | chr19:21820675-21833812 | Weak transcription Enhancers | TF binding region | 2 gene(s) | inside rSNPs | diseases |
17 | nsv833783 | chr19:21821406-21991838 | ZNF genes & repeats Strong transcription Weak transcription Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 12 gene(s) | inside rSNPs | diseases |
18 | esv3389304 | chr19:21823012-21830610 | Weak transcription Enhancers | n/a | n/a | inside rSNPs | diseases |
19 | esv11535 | chr19:21824680-21833833 | Weak transcription Enhancers | n/a | n/a | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr19:21817200-21827200 | Weak transcription | iPS DF 19.11 Cell Line | embryonic stem cell |
2 | chr19:21817400-21827200 | Weak transcription | Fetal Intestine Small | intestine |
3 | chr19:21818000-21840000 | Weak transcription | Pancreas | Pancrea |