Variant report
Variant | rs1901856 |
---|---|
Chromosome Location | chr11:59219693-59219694 |
allele | G/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] |
---|---|
rs1026320 | 0.84[EUR][1000 genomes] |
rs10736699 | 0.88[EUR][1000 genomes] |
rs10750922 | 0.84[EUR][1000 genomes] |
rs10896974 | 0.88[EUR][1000 genomes] |
rs11229957 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs11229958 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs11602856 | 0.85[EUR][1000 genomes] |
rs11604216 | 0.86[EUR][1000 genomes] |
rs11605288 | 0.85[EUR][1000 genomes] |
rs11605552 | 0.81[AMR][1000 genomes];0.92[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs11606927 | 0.85[EUR][1000 genomes] |
rs11606980 | 0.84[EUR][1000 genomes] |
rs12420159 | 0.85[EUR][1000 genomes] |
rs12785234 | 0.85[EUR][1000 genomes] |
rs1349777 | 0.85[EUR][1000 genomes] |
rs1453541 | 0.80[AMR][1000 genomes];0.92[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs1453542 | 0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs1453544 | 0.87[EUR][1000 genomes] |
rs1453547 | 0.84[EUR][1000 genomes] |
rs1453549 | 0.85[EUR][1000 genomes] |
rs1453550 | 0.85[EUR][1000 genomes] |
rs1453551 | 0.85[EUR][1000 genomes] |
rs1453552 | 0.85[EUR][1000 genomes] |
rs17500478 | 0.87[EUR][1000 genomes] |
rs17591107 | 0.87[EUR][1000 genomes] |
rs1879929 | 0.85[EUR][1000 genomes] |
rs1901855 | 0.83[AMR][1000 genomes];0.93[EUR][1000 genomes];0.95[ASN][1000 genomes] |
rs2167923 | 0.82[EUR][1000 genomes] |
rs2867731 | 0.87[EUR][1000 genomes] |
rs2867748 | 0.80[AMR][1000 genomes];0.91[EUR][1000 genomes] |
rs35630700 | 0.85[EUR][1000 genomes] |
rs4939291 | 0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes] |
rs61901576 | 0.85[EUR][1000 genomes] |
rs61901620 | 0.87[EUR][1000 genomes] |
rs61902559 | 0.86[EUR][1000 genomes] |
rs6591536 | 0.88[EUR][1000 genomes] |
rs7119928 | 0.87[EUR][1000 genomes] |
rs7120797 | 0.87[EUR][1000 genomes] |
rs7935959 | 0.85[EUR][1000 genomes] |
rs7941591 | 0.88[EUR][1000 genomes] |
rs7943953 | 0.88[EUR][1000 genomes] |
rs7947471 | 0.87[EUR][1000 genomes] |
rs7952071 | 0.86[AMR][1000 genomes];0.99[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs896877 | 0.87[EUR][1000 genomes] |
rs896878 | 0.87[EUR][1000 genomes] |
rs9665874 | 0.80[AMR][1000 genomes];0.91[EUR][1000 genomes] |
rs9787928 | 0.85[EUR][1000 genomes] |
rs9988851 | 0.84[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv1050013 | chr11:58394598-59221090 | Active TSS Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer ZNF genes & repeats Genic enhancers Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 67 gene(s) | inside rSNPs | diseases |
2 | nsv1046084 | chr11:59034871-59314519 | Enhancers Active TSS Flanking Active TSS Weak transcription ZNF genes & repeats Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 24 gene(s) | inside rSNPs | diseases |
3 | nsv1047952 | chr11:59124719-59221606 | Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats | TF binding regionCpG islandChromatin interactive region | 6 gene(s) | inside rSNPs | diseases |
4 | nsv983153 | chr11:59197223-59222105 | Enhancers Active TSS Weak transcription ZNF genes & repeats | TF binding regionCpG islandChromatin interactive region | 3 gene(s) | inside rSNPs | diseases |
5 | nsv975342 | chr11:59203908-59237268 | Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Active TSS | TF binding regionCpG island | 3 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr11:59219600-59220800 | Weak transcription | iPS DF 19.11 Cell Line | embryonic stem cell |