Variant report
Variant | rs13073423 |
---|---|
Chromosome Location | chr3:88714434-88714435 |
allele | A/C |
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] |
---|---|
rs10446361 | 1.00[AMR][1000 genomes];0.91[EUR][1000 genomes] |
rs13060621 | 0.92[AMR][1000 genomes];0.87[EUR][1000 genomes] |
rs13063234 | 0.90[ASN][1000 genomes] |
rs13063905 | 1.00[AMR][1000 genomes];0.83[EUR][1000 genomes] |
rs13067884 | 1.00[AMR][1000 genomes];0.83[EUR][1000 genomes] |
rs13068692 | 0.83[AFR][1000 genomes];1.00[AMR][1000 genomes];0.94[EUR][1000 genomes];0.90[ASN][1000 genomes] |
rs13074030 | 1.00[AMR][1000 genomes];0.87[EUR][1000 genomes] |
rs13075366 | 1.00[AMR][1000 genomes];0.87[EUR][1000 genomes] |
rs13081387 | 1.00[AMR][1000 genomes];0.83[EUR][1000 genomes] |
rs13082178 | 1.00[AMR][1000 genomes] |
rs13082894 | 1.00[AMR][1000 genomes] |
rs13083673 | 1.00[AMR][1000 genomes] |
rs13085293 | 1.00[AMR][1000 genomes];0.91[EUR][1000 genomes];0.90[ASN][1000 genomes] |
rs13088227 | 0.92[AMR][1000 genomes] |
rs13089927 | 0.96[AMR][1000 genomes];0.81[EUR][1000 genomes] |
rs13090780 | 0.92[AMR][1000 genomes] |
rs13090965 | 1.00[AMR][1000 genomes];0.83[EUR][1000 genomes] |
rs13100049 | 0.81[AFR][1000 genomes];1.00[AMR][1000 genomes];0.91[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs13100970 | 1.00[AMR][1000 genomes] |
rs17025980 | 0.92[AMR][1000 genomes] |
rs35129035 | 1.00[AMR][1000 genomes];0.87[EUR][1000 genomes] |
rs36031826 | 0.92[AMR][1000 genomes] |
rs71628821 | 0.92[AMR][1000 genomes] |
rs955291 | 0.92[AMR][1000 genomes] |
rs9820989 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv916330 | chr3:88083580-88884125 | Genic enhancers Weak transcription Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 22 gene(s) | inside rSNPs | diseases |
2 | nsv1014703 | chr3:88623532-88733631 | Enhancers Weak transcription ZNF genes & repeats Active TSS | TF binding regionChromatin interactive regionlncRNA | 1 gene(s) | inside rSNPs | diseases |
3 | nsv877156 | chr3:88690163-88803526 | Weak transcription Enhancers ZNF genes & repeats Active TSS | Chromatin interactive region | n/a | inside rSNPs | diseases |
4 | nsv877157 | chr3:88690163-88974863 | Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription | Chromatin interactive region | n/a | inside rSNPs | diseases |
5 | nsv1009261 | chr3:88700735-88754260 | Weak transcription Enhancers Active TSS ZNF genes & repeats | Chromatin interactive region | n/a | inside rSNPs | diseases |
6 | nsv536636 | chr3:88700735-88754260 | Enhancers Weak transcription ZNF genes & repeats Active TSS | Chromatin interactive region | n/a | inside rSNPs | diseases |
7 | nsv965408 | chr3:88700788-88716041 | Weak transcription Enhancers | Chromatin interactive region | n/a | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr3:88713800-88717200 | Weak transcription | hESC Derived CD56+ Ectoderm Cultured Cells | ES cell derived |