Variant report
| Variant | rs60892030 |
|---|---|
| Chromosome Location | chr7:14090218-14090219 |
| allele | G/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 | chr7:14028438..14030730-chr7:14088561..14090365,2 | K562 | blood: |
| No data |
| No data |
| No data |
| Variant related genes | Relation type |
|---|---|
| ENSG00000006468 | Chromatin interaction |
rSNPs within LD-proxies of this variant (count:25)
| rs_ID | r2[population] |
|---|---|
| rs11977259 | 0.82[ASN][1000 genomes] |
| rs12531536 | 0.84[EUR][1000 genomes] |
| rs12532319 | 0.84[ASN][1000 genomes] |
| rs12535946 | 1.00[EUR][1000 genomes] |
| rs12537436 | 1.00[EUR][1000 genomes] |
| rs12539144 | 1.00[EUR][1000 genomes] |
| rs17517039 | 0.89[EUR][1000 genomes] |
| rs2190067 | 1.00[EUR][1000 genomes] |
| rs56062513 | 0.84[ASN][1000 genomes] |
| rs58711075 | 0.89[EUR][1000 genomes] |
| rs59046742 | 0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes] |
| rs59264572 | 0.87[EUR][1000 genomes] |
| rs60290474 | 0.84[ASN][1000 genomes] |
| rs60732622 | 1.00[EUR][1000 genomes];0.95[ASN][1000 genomes] |
| rs73679253 | 0.89[EUR][1000 genomes] |
| rs73679254 | 0.82[EUR][1000 genomes] |
| rs73679255 | 0.89[EUR][1000 genomes] |
| rs73679259 | 1.00[EUR][1000 genomes] |
| rs73679269 | 0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes] |
| rs73679271 | 0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes] |
| rs73679272 | 0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes] |
| rs73679274 | 0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.91[ASN][1000 genomes] |
| rs73679276 | 0.86[AMR][1000 genomes];0.87[EUR][1000 genomes];0.93[ASN][1000 genomes] |
| rs7779975 | 0.84[ASN][1000 genomes] |
| rs7803279 | 0.84[EUR][1000 genomes] |
Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page:
1
| No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
|---|---|---|---|---|---|---|---|
| 1 | nsv1019873 | chr7:13707148-14133367 | Bivalent Enhancer Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 6 gene(s) | inside rSNPs | diseases |
| 2 | nsv949467 | chr7:13938464-14279074 | Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 5 gene(s) | inside rSNPs | diseases |
| 3 | nsv949033 | chr7:14086106-14860323 | Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 8 gene(s) | inside rSNPs | diseases |
| No data |
Chromatin state (count:0 , 50 per page) page:
| No data |
