Variant report
| Variant | rs1684913 |
|---|---|
| Chromosome Location | chr10:61687417-61687418 |
| allele | C/T |
| Outlinks | Ensembl UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:1)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
| No data |
| No data |
(count:1 , 50 per page) page:
1
| No. | Distal block | Cell Line | Cell type | Cell Stage |
|---|---|---|---|---|
| 1 | chr10:61665644..61668376-chr10:61685930..61687713,2 | K562 | blood: |
| No data |
| No data |
| No data |
| Variant related genes | Relation type |
|---|---|
| ENSG00000108091 | Chromatin interaction |
rSNPs within LD-proxies of this variant (count:11)
| rs_ID | r2[population] |
|---|---|
| rs1008887 | 0.82[ASN][1000 genomes] |
| rs1171832 | 0.81[AFR][1000 genomes] |
| rs1171849 | 0.81[ASN][1000 genomes] |
| rs1184593 | 0.80[EUR][1000 genomes];0.90[ASN][1000 genomes] |
| rs1664275 | 0.82[EUR][1000 genomes];0.92[ASN][1000 genomes] |
| rs3099370 | 0.81[EUR][1000 genomes];0.92[ASN][1000 genomes] |
| rs3099371 | 0.81[EUR][1000 genomes];0.92[ASN][1000 genomes] |
| rs6479670 | 0.84[ASN][1000 genomes] |
| rs6479675 | 0.82[ASN][1000 genomes] |
| rs7893603 | 0.84[ASN][1000 genomes] |
| rs978353 | 0.97[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes] |
Variant overlapped rSNPs/rCNVs (count:1 , 50 per page) page:
1
| No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
|---|---|---|---|---|---|---|---|
| 1 | esv1800316 | chr10:61639599-61700473 | Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats | TF binding regionCpG islandChromatin interactive region | 8 gene(s) | inside rSNPs | diseases |
| No data |
Chromatin state (count:0 , 50 per page) page:
| No data |
