Variant report
Variant | rs1462306 |
---|---|
Chromosome Location | chr3:110472041-110472042 |
allele | C/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] |
---|---|
rs10934065 | 0.90[EUR][1000 genomes] |
rs1156330 | 0.90[AMR][1000 genomes];0.98[EUR][1000 genomes] |
rs1156743 | 0.90[EUR][1000 genomes] |
rs1156744 | 0.89[EUR][1000 genomes] |
rs1156775 | 0.89[AMR][1000 genomes];0.98[EUR][1000 genomes] |
rs1156776 | 0.89[AMR][1000 genomes];0.97[EUR][1000 genomes] |
rs1156777 | 0.94[AMR][1000 genomes];0.98[EUR][1000 genomes] |
rs11925026 | 0.83[ASN][1000 genomes] |
rs12053901 | 0.83[ASN][1000 genomes] |
rs1303902 | 0.89[EUR][1000 genomes] |
rs13098266 | 0.81[EUR][1000 genomes] |
rs13098277 | 0.90[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs1350929 | 0.93[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes] |
rs1381604 | 0.87[AMR][1000 genomes];0.90[EUR][1000 genomes] |
rs1462294 | 0.88[AMR][1000 genomes];0.96[EUR][1000 genomes] |
rs1462295 | 0.83[ASN][1000 genomes] |
rs1462301 | 0.94[AMR][1000 genomes];0.93[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs1462302 | 0.93[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes] |
rs1462303 | 0.90[AMR][1000 genomes];0.97[EUR][1000 genomes] |
rs1462314 | 0.90[EUR][1000 genomes] |
rs1462315 | 0.91[EUR][1000 genomes] |
rs1462316 | 0.85[AMR][1000 genomes];0.96[EUR][1000 genomes] |
rs1473828 | 0.88[EUR][1000 genomes] |
rs1547543 | 0.88[EUR][1000 genomes] |
rs1585559 | 0.88[AMR][1000 genomes];0.91[EUR][1000 genomes] |
rs1599569 | 0.85[AMR][1000 genomes];0.97[EUR][1000 genomes] |
rs1599570 | 0.89[EUR][1000 genomes] |
rs1599572 | 0.89[EUR][1000 genomes] |
rs1599574 | 0.88[AFR][1000 genomes];0.82[AMR][1000 genomes];0.92[EUR][1000 genomes] |
rs16845001 | 0.80[ASN][1000 genomes] |
rs17202466 | 0.90[EUR][1000 genomes] |
rs1824630 | 0.86[AMR][1000 genomes];0.96[EUR][1000 genomes] |
rs1849371 | 0.80[EUR][1000 genomes] |
rs1903678 | 0.86[AMR][1000 genomes];0.97[EUR][1000 genomes] |
rs2054375 | 0.91[EUR][1000 genomes] |
rs2126450 | 0.90[EUR][1000 genomes] |
rs2169496 | 0.91[EUR][1000 genomes] |
rs2199454 | 0.88[AMR][1000 genomes];0.97[EUR][1000 genomes] |
rs2399356 | 0.86[AMR][1000 genomes];0.95[EUR][1000 genomes] |
rs2399357 | 0.90[EUR][1000 genomes] |
rs2399361 | 0.89[AMR][1000 genomes];0.98[EUR][1000 genomes] |
rs2399362 | 0.90[AMR][1000 genomes];0.91[EUR][1000 genomes];0.86[ASN][1000 genomes] |
rs4234398 | 0.87[EUR][1000 genomes] |
rs4234400 | 0.83[AMR][1000 genomes];0.94[EUR][1000 genomes] |
rs4362750 | 0.81[AMR][1000 genomes];0.94[EUR][1000 genomes] |
rs4395426 | 0.88[EUR][1000 genomes] |
rs4410465 | 0.88[EUR][1000 genomes] |
rs4438690 | 0.86[AMR][1000 genomes];0.97[EUR][1000 genomes] |
rs4449350 | 0.88[EUR][1000 genomes] |
rs4450854 | 0.88[EUR][1000 genomes] |
rs4469006 | 0.87[EUR][1000 genomes] |
rs4481181 | 0.80[AMR][1000 genomes];0.94[EUR][1000 genomes] |
rs4547734 | 0.88[EUR][1000 genomes] |
rs4550849 | 0.88[EUR][1000 genomes] |
rs4588395 | 0.87[EUR][1000 genomes] |
rs4610259 | 0.94[AMR][1000 genomes];0.92[EUR][1000 genomes];0.86[ASN][1000 genomes] |
rs4634158 | 0.88[EUR][1000 genomes] |
rs4640600 | 0.88[EUR][1000 genomes] |
rs4682014 | 0.88[EUR][1000 genomes] |
rs4682018 | 0.83[AMR][1000 genomes];0.94[EUR][1000 genomes] |
rs4682019 | 0.91[EUR][1000 genomes] |
rs4682192 | 0.88[EUR][1000 genomes] |
rs4682193 | 0.88[EUR][1000 genomes] |
rs4682194 | 0.88[EUR][1000 genomes] |
rs4682195 | 0.88[EUR][1000 genomes] |
rs4682198 | 0.83[AMR][1000 genomes];0.94[EUR][1000 genomes] |
rs4682204 | 0.91[EUR][1000 genomes] |
rs4682205 | 0.81[AMR][1000 genomes];0.92[EUR][1000 genomes] |
rs4682206 | 0.91[EUR][1000 genomes] |
rs4682207 | 0.88[EUR][1000 genomes] |
rs55894328 | 0.86[AMR][1000 genomes];0.95[EUR][1000 genomes] |
rs56203101 | 0.90[EUR][1000 genomes] |
rs60302938 | 0.83[ASN][1000 genomes] |
rs62270134 | 0.81[ASN][1000 genomes] |
rs62271763 | 0.82[ASN][1000 genomes] |
rs62271766 | 0.83[ASN][1000 genomes] |
rs62271784 | 0.83[ASN][1000 genomes] |
rs62271785 | 0.83[ASN][1000 genomes] |
rs62271788 | 0.85[ASN][1000 genomes] |
rs62271789 | 0.85[ASN][1000 genomes] |
rs6437925 | 0.93[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes] |
rs6762150 | 0.91[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes] |
rs6772035 | 0.82[ASN][1000 genomes] |
rs6773268 | 0.89[AFR][1000 genomes];0.94[AMR][1000 genomes];0.93[EUR][1000 genomes] |
rs6784490 | 0.86[AMR][1000 genomes];0.95[EUR][1000 genomes] |
rs6805801 | 0.82[AMR][1000 genomes];0.89[EUR][1000 genomes] |
rs6809227 | 0.88[AMR][1000 genomes];0.95[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs7609852 | 0.85[ASN][1000 genomes] |
rs7615772 | 0.88[AMR][1000 genomes];0.97[EUR][1000 genomes] |
rs7619217 | 0.80[EUR][1000 genomes] |
rs7629179 | 0.85[ASN][1000 genomes] |
rs7629191 | 0.90[EUR][1000 genomes] |
rs7632974 | 0.81[ASN][1000 genomes] |
rs7633076 | 0.93[AMR][1000 genomes];0.98[EUR][1000 genomes] |
rs7633234 | 0.80[AMR][1000 genomes];0.92[EUR][1000 genomes] |
rs7633936 | 0.90[EUR][1000 genomes] |
rs7637105 | 0.87[EUR][1000 genomes] |
rs7637286 | 0.88[EUR][1000 genomes] |
rs7640594 | 0.89[AMR][1000 genomes];0.98[EUR][1000 genomes] |
rs7641379 | 0.85[ASN][1000 genomes] |
rs7647181 | 0.90[EUR][1000 genomes] |
rs7647421 | 0.89[EUR][1000 genomes] |
rs7650722 | 0.83[ASN][1000 genomes] |
rs9288913 | 0.81[AMR][1000 genomes];0.92[EUR][1000 genomes] |
rs931019 | 0.91[EUR][1000 genomes] |
rs9816253 | 0.91[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes] |
rs9820478 | 0.89[AMR][1000 genomes];0.98[EUR][1000 genomes] |
rs9825259 | 0.82[ASN][1000 genomes] |
rs9826294 | 0.88[EUR][1000 genomes] |
rs9830854 | 0.90[EUR][1000 genomes] |
rs9830959 | 0.90[AMR][1000 genomes];0.98[EUR][1000 genomes] |
rs9836371 | 0.90[EUR][1000 genomes] |
rs9837589 | 0.90[EUR][1000 genomes] |
rs9838550 | 0.83[AMR][1000 genomes];0.93[EUR][1000 genomes] |
rs9838611 | 0.88[EUR][1000 genomes] |
rs9838715 | 0.86[EUR][1000 genomes] |
rs9840671 | 0.88[EUR][1000 genomes] |
rs9842924 | 0.86[AMR][1000 genomes];0.97[EUR][1000 genomes] |
rs9843528 | 0.87[EUR][1000 genomes] |
rs9843978 | 0.88[EUR][1000 genomes] |
rs9844791 | 0.88[EUR][1000 genomes] |
rs9857065 | 0.88[AMR][1000 genomes];0.92[EUR][1000 genomes] |
rs9857228 | 0.84[EUR][1000 genomes] |
rs9858359 | 0.82[ASN][1000 genomes] |
rs9859534 | 0.82[AMR][1000 genomes];0.92[EUR][1000 genomes] |
rs9863549 | 0.88[EUR][1000 genomes] |
rs9864306 | 0.88[EUR][1000 genomes] |
rs9873714 | 0.82[ASN][1000 genomes] |
rs9876058 | 0.88[EUR][1000 genomes] |
rs9884058 | 0.88[EUR][1000 genomes] |
rs991930 | 0.88[AMR][1000 genomes];0.92[EUR][1000 genomes] |
rs994125 | 0.90[AMR][1000 genomes];0.98[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv1001810 | chr3:110158316-110522247 | Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 5 gene(s) | inside rSNPs | diseases |
2 | nsv1010230 | chr3:110204439-110588814 | Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Active TSS Strong transcription Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 5 gene(s) | inside rSNPs | diseases |
3 | nsv536688 | chr3:110204439-110588814 | Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 5 gene(s) | inside rSNPs | diseases |
4 | nsv1011034 | chr3:110209344-110559021 | Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 5 gene(s) | inside rSNPs | diseases |
5 | nsv536689 | chr3:110209344-110559021 | Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 5 gene(s) | inside rSNPs | diseases |
6 | nsv1003106 | chr3:110264476-111105943 | Weak transcription Enhancers Strong transcription Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 13 gene(s) | inside rSNPs | diseases |
7 | nsv1014199 | chr3:110293896-110754155 | Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Strong transcription Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 6 gene(s) | inside rSNPs | diseases |
8 | nsv829673 | chr3:110378069-110530815 | Enhancers Weak transcription Bivalent/Poised TSS ZNF genes & repeats Flanking Active TSS Active TSS | TF binding regionCpG islandChromatin interactive region | 2 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr3:110468200-110472800 | Weak transcription | iPS-20b Cell Line | embryonic stem cell |
2 | chr3:110468400-110473600 | Weak transcription | ES-I3 Cell Line | embryonic stem cell |
3 | chr3:110468800-110472400 | Weak transcription | HUES48 Cell Line | embryonic stem cell |
4 | chr3:110469400-110472200 | Weak transcription | Pancreatic Islets | Pancreatic Islet |
5 | chr3:110471200-110473600 | Weak transcription | H1 BMP4 Derived Mesendoderm Cultured Cells | ES cell derived |
6 | chr3:110471400-110473000 | Weak transcription | HUES64 Cell Line | embryonic stem cell |
7 | chr3:110471400-110473000 | Weak transcription | iPS-18 Cell Line | embryonic stem cell |
8 | chr3:110471400-110492200 | Weak transcription | H1 Derived Neuronal Progenitor Cultured Cells | ES cell derived |
9 | chr3:110471600-110473200 | Weak transcription | iPS-15b Cell Line | embryonic stem cell |
10 | chr3:110471600-110473400 | Weak transcription | H9 Cell Line | embryonic stem cell |
11 | chr3:110471600-110474600 | Weak transcription | ES-UCSF4 Cell Line | embryonic stem cell |