Variant report
Variant | rs73100838 |
---|---|
Chromosome Location | chr12:44600306-44600307 |
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] |
---|---|
rs10506235 | 0.88[AFR][1000 genomes] |
rs10506236 | 0.88[AFR][1000 genomes] |
rs10506239 | 0.88[AFR][1000 genomes] |
rs10506240 | 0.80[AFR][1000 genomes] |
rs10506241 | 0.95[AFR][1000 genomes] |
rs11609283 | 0.95[AFR][1000 genomes] |
rs11609568 | 0.95[AFR][1000 genomes] |
rs11610433 | 0.95[AFR][1000 genomes] |
rs11612257 | 0.95[AFR][1000 genomes] |
rs11613064 | 0.95[AFR][1000 genomes] |
rs11613444 | 0.95[AFR][1000 genomes] |
rs1527316 | 0.92[AFR][1000 genomes] |
rs17094121 | 0.88[AFR][1000 genomes] |
rs17094226 | 0.93[AFR][1000 genomes] |
rs17094228 | 0.95[AFR][1000 genomes] |
rs17094242 | 0.95[AFR][1000 genomes] |
rs17094260 | 0.95[AFR][1000 genomes] |
rs17094263 | 0.95[AFR][1000 genomes] |
rs17094282 | 0.95[AFR][1000 genomes] |
rs17094291 | 0.95[AFR][1000 genomes] |
rs17094292 | 0.95[AFR][1000 genomes] |
rs17094298 | 0.95[AFR][1000 genomes] |
rs17094299 | 0.95[AFR][1000 genomes] |
rs17094300 | 0.95[AFR][1000 genomes] |
rs17094304 | 0.95[AFR][1000 genomes] |
rs17094313 | 0.95[AFR][1000 genomes] |
rs17094322 | 0.92[AFR][1000 genomes] |
rs17094323 | 0.92[AFR][1000 genomes] |
rs17094325 | 0.92[AFR][1000 genomes] |
rs17094330 | 0.92[AFR][1000 genomes] |
rs17094336 | 0.89[AFR][1000 genomes] |
rs17094343 | 0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs17094356 | 0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs28397962 | 0.95[AFR][1000 genomes] |
rs55633842 | 0.92[AFR][1000 genomes] |
rs55645887 | 0.92[AFR][1000 genomes] |
rs55649839 | 0.84[AFR][1000 genomes] |
rs55747421 | 0.92[AFR][1000 genomes] |
rs55840982 | 0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs55874183 | 0.92[AFR][1000 genomes] |
rs55991202 | 0.92[AFR][1000 genomes] |
rs55999021 | 0.95[AFR][1000 genomes] |
rs56192803 | 0.95[AFR][1000 genomes] |
rs56218625 | 0.87[AFR][1000 genomes] |
rs56339470 | 0.89[AFR][1000 genomes] |
rs56877775 | 0.86[EUR][1000 genomes] |
rs57094207 | 0.95[AFR][1000 genomes] |
rs57851938 | 0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs58450697 | 0.92[AFR][1000 genomes] |
rs58602576 | 0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];0.86[EUR][1000 genomes] |
rs59118688 | 0.87[EUR][1000 genomes] |
rs59136483 | 0.92[AFR][1000 genomes] |
rs59618205 | 0.81[EUR][1000 genomes] |
rs59704299 | 0.92[AFR][1000 genomes] |
rs59957474 | 0.89[AFR][1000 genomes] |
rs60461380 | 0.92[AFR][1000 genomes] |
rs60939199 | 0.88[AFR][1000 genomes] |
rs61228557 | 0.95[AFR][1000 genomes] |
rs61399923 | 0.85[EUR][1000 genomes] |
rs66993609 | 0.87[EUR][1000 genomes] |
rs7305296 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs7308476 | 0.95[AFR][1000 genomes] |
rs73086766 | 0.84[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes] |
rs73093451 | 0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];0.86[EUR][1000 genomes] |
rs73093458 | 0.88[AFR][1000 genomes] |
rs73093470 | 0.86[EUR][1000 genomes] |
rs73093490 | 0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];0.86[EUR][1000 genomes] |
rs73093494 | 0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];0.86[EUR][1000 genomes] |
rs73093496 | 0.86[EUR][1000 genomes] |
rs73096886 | 0.86[EUR][1000 genomes] |
rs73099009 | 0.98[AFR][1000 genomes] |
rs73099011 | 0.98[AFR][1000 genomes] |
rs73099012 | 0.86[EUR][1000 genomes] |
rs73099027 | 0.92[AFR][1000 genomes] |
rs73100803 | 0.92[AFR][1000 genomes] |
rs73100817 | 0.92[AFR][1000 genomes] |
rs73100829 | 0.95[AFR][1000 genomes] |
rs73100835 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs73100841 | 0.84[AFR][1000 genomes] |
rs73100848 | 0.95[AFR][1000 genomes] |
rs73100851 | 0.83[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes] |
rs73102910 | 0.95[AFR][1000 genomes] |
rs73102919 | 0.95[AFR][1000 genomes] |
rs73102924 | 0.95[AFR][1000 genomes] |
rs73102925 | 0.95[AFR][1000 genomes] |
rs73102927 | 0.95[AFR][1000 genomes] |
rs73102932 | 0.92[AFR][1000 genomes] |
rs73102937 | 0.92[AFR][1000 genomes] |
rs73102938 | 0.92[AFR][1000 genomes] |
rs73102952 | 0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs73102953 | 0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes] |
rs73102954 | 0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs73102964 | 0.95[EUR][1000 genomes] |
rs7310881 | 0.95[AFR][1000 genomes] |
rs7311714 | 0.95[AFR][1000 genomes] |
rs7311937 | 0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs7313649 | 0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs7954216 | 0.92[AFR][1000 genomes] |
rs7968824 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.86[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv1049818 | chr12:44486312-45133783 | Enhancers ZNF genes & repeats Weak transcription Active TSS Strong transcription Flanking Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 6 gene(s) | inside rSNPs | diseases |
2 | nsv832393 | chr12:44529406-44692414 | Enhancers Weak transcription Active TSS Strong transcription ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Genic enhancers | TF binding regionChromatin interactive regionlncRNA | 4 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr12:44511400-44605800 | Weak transcription | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |
2 | chr12:44599600-44600400 | ZNF genes & repeats | Pancreatic Islets | Pancreatic Islet |
3 | chr12:44600000-44606000 | Weak transcription | Foreskin Melanocyte Primary Cells skin03 | Skin |
4 | chr12:44600200-44600400 | ZNF genes & repeats | Duodenum Smooth Muscle | Duodenum |
5 | chr12:44600200-44617000 | Weak transcription | Ovary | ovary |