Variant report
Variant | rs10214113 |
---|---|
Chromosome Location | chr5:28505206-28505207 |
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 |
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No data |
rs_ID | r2[population] |
---|---|
rs10038220 | 0.81[EUR][1000 genomes] |
rs10064359 | 0.92[ASN][1000 genomes] |
rs10064432 | 0.92[ASN][1000 genomes] |
rs10064470 | 0.92[ASN][1000 genomes] |
rs10064651 | 0.92[ASN][1000 genomes] |
rs10064884 | 0.92[ASN][1000 genomes] |
rs10066564 | 0.92[ASN][1000 genomes] |
rs10472130 | 0.93[ASN][1000 genomes] |
rs10472638 | 0.93[ASN][1000 genomes] |
rs13354837 | 0.93[ASN][1000 genomes] |
rs13357289 | 0.93[ASN][1000 genomes] |
rs13359620 | 0.93[ASN][1000 genomes] |
rs34334341 | 0.91[AFR][1000 genomes];0.89[AMR][1000 genomes];0.93[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs4133400 | 0.93[ASN][1000 genomes] |
rs4352606 | 0.97[AFR][1000 genomes];0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs4370283 | 0.93[ASN][1000 genomes] |
rs4608932 | 0.89[ASN][1000 genomes] |
rs4624798 | 0.90[ASN][1000 genomes] |
rs62357806 | 0.93[ASN][1000 genomes] |
rs62357807 | 0.93[ASN][1000 genomes] |
rs6870808 | 0.93[ASN][1000 genomes] |
rs6891511 | 0.81[EUR][1000 genomes] |
rs7702820 | 0.91[AFR][1000 genomes];0.86[AMR][1000 genomes];0.93[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs7710045 | 0.92[ASN][1000 genomes] |
rs7714820 | 0.93[ASN][1000 genomes] |
rs7726767 | 1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs7729885 | 0.93[ASN][1000 genomes] |
rs9292264 | 0.91[AFR][1000 genomes];0.89[AMR][1000 genomes];0.91[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs9292265 | 0.91[AFR][1000 genomes];0.89[AMR][1000 genomes];0.93[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs9292267 | 0.93[ASN][1000 genomes] |
rs9784664 | 0.90[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv880550 | chr5:27863157-28732126 | Enhancers ZNF genes & repeats Weak transcription Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 9 gene(s) | inside rSNPs | diseases |
2 | nsv1026700 | chr5:28067287-28978638 | Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 14 gene(s) | inside rSNPs | diseases |
3 | nsv537707 | chr5:28067287-28978638 | Enhancers Flanking Active TSS Weak transcription Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 14 gene(s) | inside rSNPs | diseases |
4 | nsv1029219 | chr5:28370908-29086506 | Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 13 gene(s) | inside rSNPs | diseases |
5 | nsv537710 | chr5:28370908-29086506 | Enhancers ZNF genes & repeats Weak transcription Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 13 gene(s) | inside rSNPs | diseases |
6 | nsv830242 | chr5:28489481-28660242 | Enhancers Active TSS Weak transcription ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
7 | nsv881368 | chr5:28489902-28604170 | Enhancers ZNF genes & repeats Weak transcription | Chromatin interactive regionlncRNA | 1 gene(s) | inside rSNPs | diseases |
8 | nsv881494 | chr5:28498983-28646417 | Enhancers Active TSS Weak transcription ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
9 | nsv880822 | chr5:28498983-28959648 | Enhancers Weak transcription Bivalent/Poised TSS Active TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 9 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr5:28505000-28505600 | Enhancers | Breast Myoepithelial Primary Cells | Breast |
2 | chr5:28505200-28506000 | Enhancers | Hela-S3 | cervix |