Variant report
Variant | rs73052931 |
---|---|
Chromosome Location | chr1:194190075-194190076 |
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] |
---|---|
rs1487527 | 0.84[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs16836190 | 1.00[AMR][1000 genomes] |
rs16836491 | 0.90[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs16836545 | 0.96[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs16836597 | 0.90[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs56695737 | 0.90[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs60277362 | 0.90[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs60574560 | 1.00[AMR][1000 genomes] |
rs60860075 | 1.00[AMR][1000 genomes] |
rs73052905 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs73052916 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs73052919 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs73052935 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs73052944 | 0.96[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs73053002 | 0.90[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs73055004 | 0.96[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs73055015 | 0.96[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs73056909 | 0.90[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs73056916 | 0.90[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs73056918 | 0.90[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs73056925 | 0.90[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs73056944 | 0.90[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs73064707 | 1.00[AMR][1000 genomes] |
rs73064728 | 1.00[AMR][1000 genomes] |
rs73070728 | 0.84[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs73070733 | 0.84[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs73070741 | 0.84[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs73070750 | 0.84[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs73070753 | 0.90[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs73070757 | 0.90[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs73070766 | 0.90[AFR][1000 genomes];1.00[AMR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv1008266 | chr1:193550185-194481053 | Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer Strong transcription Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 9 gene(s) | inside rSNPs | diseases |
2 | nsv872834 | chr1:193889533-194482304 | Enhancers ZNF genes & repeats Flanking Active TSS Weak transcription Strong transcription Active TSS Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 5 gene(s) | inside rSNPs | diseases |
3 | nsv1001872 | chr1:194030479-194288016 | Active TSS Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 3 gene(s) | inside rSNPs | diseases |
4 | nsv832181 | chr1:194089117-194255615 | Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer | TF binding regionChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
5 | nsv872837 | chr1:194106280-194221509 | Active TSS Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Bivalent Enhancer Strong transcription | TF binding regionChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
6 | nsv1004338 | chr1:194143315-194381135 | Enhancers ZNF genes & repeats Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
7 | esv3368503 | chr1:194188279-194190177 | Flanking Active TSS Weak transcription Enhancers | n/a | n/a | inside rSNPs | n/a |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr1:194159400-194195200 | Weak transcription | Thymus | Thymus |
2 | chr1:194184000-194195400 | Weak transcription | Fetal Thymus | thymus |
3 | chr1:194187000-194194600 | Weak transcription | Primary T cells effector/memory enriched fromperipheralblood | blood |