Variant report
| Variant | rs7975125 |
|---|---|
| Chromosome Location | chr12:105645519-105645520 |
| 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 | chr12:105629810..105631890-chr12:105644832..105647203,2 | MCF-7 | breast: |
| No data |
| No data |
| No data |
| Variant related genes | Relation type |
|---|---|
| ENSG00000136044 | Chromatin interaction |
rSNPs within LD-proxies of this variant (count:25)
| rs_ID | r2[population] |
|---|---|
| rs10778370 | 0.84[ASN][1000 genomes] |
| rs10778376 | 0.80[ASN][1000 genomes] |
| rs10861365 | 0.83[AFR][1000 genomes];0.86[ASN][1000 genomes] |
| rs10861366 | 0.81[ASN][1000 genomes] |
| rs10861368 | 0.81[ASN][1000 genomes] |
| rs10861369 | 0.81[ASN][1000 genomes] |
| rs11112418 | 0.99[ASN][1000 genomes] |
| rs11112422 | 0.97[ASN][1000 genomes] |
| rs11112435 | 0.81[AFR][1000 genomes];0.86[ASN][1000 genomes] |
| rs11112441 | 0.81[ASN][1000 genomes] |
| rs12306463 | 0.80[ASN][1000 genomes] |
| rs12316054 | 0.80[ASN][1000 genomes] |
| rs12322134 | 0.99[ASN][1000 genomes] |
| rs12425893 | 0.85[EUR][1000 genomes] |
| rs3794232 | 0.99[ASN][1000 genomes] |
| rs3794237 | 0.84[ASN][1000 genomes] |
| rs56043130 | 0.80[ASN][1000 genomes] |
| rs6539199 | 0.80[ASN][1000 genomes] |
| rs7138073 | 0.80[ASN][1000 genomes] |
| rs7488014 | 0.88[ASN][1000 genomes] |
| rs7955095 | 0.81[ASN][1000 genomes] |
| rs7966106 | 0.99[ASN][1000 genomes] |
| rs7972263 | 0.81[ASN][1000 genomes] |
| rs7975197 | 0.80[ASN][1000 genomes] |
| rs9634185 | 0.99[ASN][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 | nsv455704 | chr12:105583877-105651356 | Strong transcription Weak transcription Active TSS Enhancers Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats | TF binding regionCpG islandChromatin interactive region | 15 gene(s) | inside rSNPs | diseases |
| 2 | nsv560053 | chr12:105583877-105651356 | Genic enhancers Strong transcription Flanking Active TSS Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer | TF binding regionCpG islandChromatin interactive region | 15 gene(s) | inside rSNPs | diseases |
| 3 | nsv899499 | chr12:105616297-105722529 | Bivalent Enhancer Enhancers Weak transcription Active TSS Flanking Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 17 gene(s) | inside rSNPs | diseases |
| No data |
Chromatin state (count:0 , 50 per page) page:
| No data |
