Variant report
Variant | rs640610 |
---|---|
Chromosome Location | chr2:72650937-72650938 |
allele | A/G |
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] |
---|---|
rs10168145 | 1.00[CHB][hapmap] |
rs10173381 | 1.00[CEU][hapmap];1.00[CHB][hapmap];0.83[AMR][1000 genomes];0.85[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs10183056 | 1.00[CHB][hapmap] |
rs10186080 | 1.00[CHB][hapmap] |
rs10190674 | 1.00[CHB][hapmap] |
rs10192800 | 1.00[CHB][hapmap] |
rs10194216 | 0.82[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs10203965 | 1.00[CHB][hapmap] |
rs10204415 | 1.00[CHB][hapmap] |
rs10206555 | 1.00[CHB][hapmap] |
rs10207299 | 1.00[CHB][hapmap] |
rs10460572 | 1.00[CHB][hapmap] |
rs10865391 | 1.00[CHB][hapmap] |
rs11126366 | 1.00[CEU][hapmap];1.00[CHB][hapmap];0.85[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs11126370 | 1.00[CHB][hapmap] |
rs11126373 | 1.00[CHB][hapmap] |
rs11126374 | 1.00[CHB][hapmap] |
rs11126376 | 1.00[CHB][hapmap];1.00[ASN][1000 genomes] |
rs11686713 | 1.00[CHB][hapmap];1.00[ASN][1000 genomes] |
rs11690734 | 1.00[CHB][hapmap] |
rs11694921 | 1.00[CHB][hapmap] |
rs11889717 | 1.00[YRI][hapmap] |
rs11895324 | 1.00[YRI][hapmap] |
rs11902025 | 1.00[CHB][hapmap] |
rs11902465 | 1.00[YRI][hapmap] |
rs11902636 | 0.83[YRI][hapmap] |
rs12052508 | 1.00[CHB][hapmap];1.00[ASN][1000 genomes] |
rs12466613 | 1.00[CHB][hapmap] |
rs12467816 | 1.00[CHB][hapmap] |
rs12468057 | 1.00[CEU][hapmap];1.00[CHB][hapmap];0.83[EUR][1000 genomes] |
rs12471136 | 1.00[CHB][hapmap] |
rs12471312 | 1.00[CHB][hapmap];1.00[ASN][1000 genomes] |
rs12471875 | 1.00[CHB][hapmap] |
rs12476130 | 1.00[CHB][hapmap] |
rs12476397 | 1.00[CHB][hapmap] |
rs12618390 | 1.00[CHB][hapmap] |
rs12713772 | 1.00[CHB][hapmap] |
rs12713773 | 1.00[CHB][hapmap] |
rs12713774 | 1.00[CHB][hapmap] |
rs12992973 | 1.00[CHB][hapmap];1.00[ASN][1000 genomes] |
rs12996319 | 1.00[CHB][hapmap] |
rs12998681 | 1.00[CHB][hapmap] |
rs13008041 | 1.00[CHB][hapmap] |
rs13008258 | 1.00[CHB][hapmap] |
rs13011477 | 1.00[CHB][hapmap];1.00[ASN][1000 genomes] |
rs13383535 | 1.00[CHB][hapmap] |
rs13390754 | 1.00[CEU][hapmap];1.00[CHB][hapmap];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs13409513 | 1.00[CHB][hapmap] |
rs13409641 | 1.00[CHB][hapmap] |
rs13432350 | 1.00[CHB][hapmap] |
rs1400581 | 1.00[CHB][hapmap];1.00[ASN][1000 genomes] |
rs1400582 | 1.00[CHB][hapmap] |
rs1446888 | 1.00[CHB][hapmap] |
rs1446890 | 1.00[CHB][hapmap] |
rs1446891 | 1.00[CHB][hapmap] |
rs1446892 | 1.00[CHB][hapmap] |
rs1446893 | 1.00[CHB][hapmap] |
rs1517181 | 1.00[CHB][hapmap] |
rs1517185 | 1.00[CHB][hapmap];1.00[ASN][1000 genomes] |
rs1568145 | 1.00[CHB][hapmap] |
rs1596930 | 1.00[CHB][hapmap];1.00[ASN][1000 genomes] |
rs1596931 | 1.00[CHB][hapmap];1.00[ASN][1000 genomes] |
rs1711838 | 1.00[CHB][hapmap] |
rs1947118 | 1.00[ASN][1000 genomes] |
rs2109960 | 1.00[CHB][hapmap] |
rs2138683 | 1.00[CHB][hapmap] |
rs2192014 | 1.00[CHB][hapmap] |
rs2192015 | 1.00[CHB][hapmap] |
rs2203679 | 1.00[CHB][hapmap];1.00[ASN][1000 genomes] |
rs2420444 | 1.00[CEU][hapmap];1.00[CHB][hapmap];0.83[AMR][1000 genomes];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs2901146 | 1.00[CHB][hapmap];1.00[ASN][1000 genomes] |
rs3115351 | 1.00[CEU][hapmap];1.00[CHB][hapmap];0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs4364045 | 1.00[CHB][hapmap];1.00[ASN][1000 genomes] |
rs4852286 | 1.00[CHB][hapmap] |
rs4852287 | 1.00[CHB][hapmap] |
rs4852288 | 1.00[CHB][hapmap] |
rs4852291 | 1.00[CHB][hapmap] |
rs4852292 | 1.00[CHB][hapmap] |
rs4852293 | 1.00[CHB][hapmap] |
rs4852872 | 1.00[CHB][hapmap] |
rs4852873 | 1.00[CHB][hapmap];1.00[ASN][1000 genomes] |
rs4852874 | 1.00[CHB][hapmap];1.00[ASN][1000 genomes] |
rs4852875 | 1.00[CHB][hapmap] |
rs4852876 | 1.00[CHB][hapmap] |
rs4852877 | 1.00[CHB][hapmap] |
rs4852878 | 1.00[CHB][hapmap] |
rs4852880 | 1.00[CHB][hapmap] |
rs4852883 | 1.00[ASN][1000 genomes] |
rs57270251 | 0.85[EUR][1000 genomes] |
rs583119 | 0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs583673 | 1.00[CHB][hapmap] |
rs584522 | 0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs585653 | 1.00[CHB][hapmap] |
rs585938 | 1.00[CHB][hapmap] |
rs587431 | 1.00[CHB][hapmap] |
rs587744 | 1.00[CEU][hapmap];1.00[CHB][hapmap];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs589547 | 1.00[CHB][hapmap];1.00[ASN][1000 genomes] |
rs590252 | 1.00[CEU][hapmap];1.00[CHB][hapmap];0.81[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs590345 | 1.00[CHB][hapmap];1.00[ASN][1000 genomes] |
rs598138 | 1.00[CEU][hapmap];1.00[CHB][hapmap];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs598496 | 1.00[CEU][hapmap];1.00[CHB][hapmap];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs602465 | 1.00[CHB][hapmap] |
rs613880 | 1.00[CHB][hapmap] |
rs614653 | 1.00[CHB][hapmap] |
rs620770 | 1.00[ASN][1000 genomes] |
rs625434 | 1.00[CHB][hapmap] |
rs628432 | 1.00[CEU][hapmap];1.00[CHB][hapmap];0.85[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs630241 | 1.00[CEU][hapmap];1.00[CHB][hapmap];0.81[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs632670 | 1.00[CHB][hapmap] |
rs634476 | 1.00[CHB][hapmap] |
rs634574 | 1.00[CHB][hapmap] |
rs634586 | 1.00[ASN][1000 genomes] |
rs634785 | 1.00[CHB][hapmap] |
rs634929 | 1.00[CHB][hapmap] |
rs636319 | 1.00[CHB][hapmap] |
rs636734 | 1.00[CHB][hapmap] |
rs638854 | 1.00[CEU][hapmap];1.00[CHB][hapmap];0.81[AMR][1000 genomes];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs641123 | 1.00[CHB][hapmap] |
rs641939 | 1.00[CEU][hapmap];1.00[CHB][hapmap];0.86[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs642652 | 1.00[CEU][hapmap];1.00[CHB][hapmap];0.85[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs645489 | 1.00[CHB][hapmap] |
rs646357 | 1.00[CHB][hapmap] |
rs647242 | 1.00[CHB][hapmap];1.00[ASN][1000 genomes] |
rs647269 | 1.00[CHB][hapmap] |
rs650352 | 1.00[CHB][hapmap] |
rs653220 | 1.00[CHB][hapmap];1.00[ASN][1000 genomes] |
rs6546756 | 1.00[CHB][hapmap] |
rs6546759 | 0.83[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs6546760 | 0.94[CEU][hapmap];1.00[CHB][hapmap];1.00[ASN][1000 genomes] |
rs6546764 | 1.00[CEU][hapmap];1.00[CHB][hapmap];0.85[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs6546765 | 1.00[CHB][hapmap] |
rs6546777 | 1.00[CHB][hapmap] |
rs6546778 | 1.00[CHB][hapmap] |
rs6546779 | 1.00[CHB][hapmap] |
rs656370 | 1.00[CHB][hapmap] |
rs656440 | 1.00[CHB][hapmap] |
rs658067 | 1.00[CHB][hapmap] |
rs659833 | 1.00[CEU][hapmap];1.00[CHB][hapmap];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs663218 | 1.00[CEU][hapmap];1.00[CHB][hapmap];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs666233 | 1.00[CEU][hapmap];1.00[CHB][hapmap];0.84[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs666361 | 1.00[CHB][hapmap] |
rs668586 | 1.00[ASN][1000 genomes] |
rs669074 | 1.00[CHB][hapmap] |
rs6711265 | 1.00[ASN][1000 genomes] |
rs6714312 | 0.85[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs6714419 | 1.00[ASN][1000 genomes] |
rs6714595 | 1.00[CHB][hapmap];1.00[ASN][1000 genomes] |
rs671721 | 1.00[CHB][hapmap] |
rs6729863 | 1.00[CHB][hapmap] |
rs6733210 | 1.00[CHB][hapmap] |
rs6737565 | 0.85[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs6742264 | 1.00[CHB][hapmap] |
rs6742312 | 1.00[CHB][hapmap] |
rs6747378 | 1.00[CHB][hapmap] |
rs674863 | 1.00[CHB][hapmap] |
rs6750766 | 1.00[CHB][hapmap] |
rs6752122 | 1.00[CEU][hapmap];1.00[CHB][hapmap];0.83[AMR][1000 genomes];0.85[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs6753073 | 1.00[CHB][hapmap] |
rs6758462 | 1.00[CHB][hapmap] |
rs6758593 | 1.00[CHB][hapmap];1.00[ASN][1000 genomes] |
rs678684 | 1.00[CHB][hapmap] |
rs680380 | 1.00[CHB][hapmap] |
rs680495 | 1.00[CEU][hapmap];1.00[CHB][hapmap];0.86[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs681574 | 1.00[CHB][hapmap] |
rs683328 | 1.00[CHB][hapmap] |
rs684673 | 1.00[CHB][hapmap] |
rs687325 | 1.00[CHB][hapmap] |
rs687371 | 1.00[CHB][hapmap] |
rs688433 | 1.00[CHB][hapmap] |
rs689154 | 1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs7420588 | 0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs7420667 | 1.00[CHB][hapmap];1.00[ASN][1000 genomes] |
rs7558686 | 1.00[CEU][hapmap];1.00[CHB][hapmap];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs7558919 | 1.00[CEU][hapmap];1.00[CHB][hapmap];0.85[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs7559131 | 1.00[CHB][hapmap] |
rs7560529 | 1.00[CHB][hapmap] |
rs7563738 | 1.00[ASN][1000 genomes] |
rs7565198 | 1.00[CHB][hapmap] |
rs7568803 | 1.00[CEU][hapmap];1.00[CHB][hapmap];0.82[AMR][1000 genomes];0.85[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs7577238 | 1.00[CHB][hapmap] |
rs7577877 | 1.00[CEU][hapmap];1.00[CHB][hapmap] |
rs7580952 | 1.00[ASN][1000 genomes] |
rs7583271 | 1.00[CHB][hapmap] |
rs7591025 | 1.00[CHB][hapmap] |
rs7591303 | 1.00[CHB][hapmap] |
rs7594350 | 1.00[CEU][hapmap];1.00[CHB][hapmap];0.83[AMR][1000 genomes];0.85[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs7595180 | 0.94[CEU][hapmap];1.00[CHB][hapmap];1.00[ASN][1000 genomes] |
rs7595315 | 0.83[AMR][1000 genomes];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs7598238 | 1.00[CHB][hapmap] |
rs7600273 | 1.00[ASN][1000 genomes] |
rs7601020 | 1.00[CHB][hapmap] |
rs7601318 | 1.00[CHB][hapmap] |
rs7603966 | 1.00[CHB][hapmap] |
rs9309464 | 1.00[CEU][hapmap];1.00[CHB][hapmap];0.85[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs983928 | 1.00[CHB][hapmap] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv963919 | chr2:72372956-72830387 | Enhancers Strong transcription Weak transcription Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 3 gene(s) | inside rSNPs | diseases |
2 | nsv1005487 | chr2:72464784-72819704 | Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Strong transcription Active TSS Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
3 | nsv999179 | chr2:72561463-72761103 | Strong transcription Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Genic enhancers Bivalent Enhancer | TF binding regionCpG islandChromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
4 | nsv1008335 | chr2:72561463-72819704 | ZNF genes & repeats Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS Genic enhancers Bivalent Enhancer | TF binding regionCpG islandChromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
5 | nsv874264 | chr2:72593243-72901170 | Weak transcription Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Active TSS Genic enhancers Bivalent Enhancer | TF binding regionCpG islandChromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr2:72613800-72654000 | Weak transcription | Foreskin Keratinocyte Primary Cells skin02 | Skin |
2 | chr2:72636200-72654000 | Weak transcription | Aorta | Aorta |
3 | chr2:72638800-72655400 | Weak transcription | Left Ventricle | heart |
4 | chr2:72641800-72654200 | Weak transcription | Fetal Stomach | stomach |
5 | chr2:72647400-72654000 | Weak transcription | H1 Derived Mesenchymal Stem Cells | ES cell derived |
6 | chr2:72647400-72688800 | Weak transcription | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |
7 | chr2:72648600-72657200 | Weak transcription | Skeletal Muscle Male | skeletal muscle |
8 | chr2:72649000-72653800 | Weak transcription | Pancreas | Pancrea |
9 | chr2:72649400-72654200 | Weak transcription | Esophagus | oesophagus |
10 | chr2:72649600-72654200 | Weak transcription | Foreskin Keratinocyte Primary Cells skin03 | Skin |
11 | chr2:72650400-72659600 | Weak transcription | Fetal Intestine Small | intestine |
12 | chr2:72650600-72651600 | Enhancers | Mesenchymal Stem Cell Derived Adipocyte Cultured Cells | ES cell derived |
13 | chr2:72650800-72651000 | Enhancers | H1 Derived Neuronal Progenitor Cultured Cells | ES cell derived |