Variant report
| Variant | rs4749254 |
|---|---|
| Chromosome Location | chr10:27931136-27931137 |
| 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 |
rSNPs within LD-proxies of this variant (count:25)
| rs_ID | r2[population] |
|---|---|
| rs10829295 | 0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes] |
| rs11015919 | 0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes] |
| rs11015924 | 0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes] |
| rs11015933 | 1.00[ASN][1000 genomes] |
| rs12260084 | 0.85[AFR][1000 genomes];0.87[EUR][1000 genomes] |
| rs1552878 | 0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes] |
| rs3952833 | 0.98[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes] |
| rs4749258 | 0.97[ASN][1000 genomes] |
| rs60014356 | 0.99[ASN][1000 genomes] |
| rs60891419 | 1.00[ASN][1000 genomes] |
| rs6482635 | 0.91[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes] |
| rs7069754 | 0.84[EUR][1000 genomes] |
| rs7076663 | 0.86[AFR][1000 genomes];0.87[EUR][1000 genomes] |
| rs7082165 | 0.95[ASN][1000 genomes] |
| rs7083092 | 0.91[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes] |
| rs7089354 | 0.82[EUR][1000 genomes] |
| rs7092214 | 0.85[AFR][1000 genomes];0.87[EUR][1000 genomes] |
| rs7100202 | 0.82[EUR][1000 genomes] |
| rs72629769 | 0.82[EUR][1000 genomes] |
| rs7893641 | 0.82[EUR][1000 genomes] |
| rs7902371 | 0.94[ASN][1000 genomes] |
| rs7908497 | 0.87[EUR][1000 genomes] |
| rs7920770 | 0.98[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
| rs9804393 | 0.85[AFR][1000 genomes];0.82[EUR][1000 genomes] |
| rs9804407 | 0.86[AFR][1000 genomes];0.87[EUR][1000 genomes] |
Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page:
1
| No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
|---|---|---|---|---|---|---|---|
| 1 | nsv550241 | chr10:27569521-28025771 | Enhancers ZNF genes & repeats Strong transcription Weak transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 27 gene(s) | inside rSNPs | diseases |
| 2 | esv3368825 | chr10:27864181-28043820 | Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer Bivalent/Poised TSS Active TSS ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 2 gene(s) | inside rSNPs | diseases |
| 3 | nsv894985 | chr10:27869503-27957785 | Bivalent Enhancer Enhancers Active TSS Weak transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS | Chromatin interactive region | n/a | inside rSNPs | diseases |
| 4 | nsv894986 | chr10:27904646-27957785 | Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh | Chromatin interactive region | n/a | inside rSNPs | diseases |
| 5 | esv3362263 | chr10:27929908-27934180 | Weak transcription Flanking Active TSS Enhancers | n/a | n/a | inside rSNPs | diseases |
| No data |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr10:27927200-27932200 | Weak transcription | Osteobl | bone |
| 2 | chr10:27927400-27932000 | Weak transcription | HSMMtube | muscle |
| 3 | chr10:27927800-27932200 | Weak transcription | Adipose Nuclei | Adipose |
