Variant report
| Variant | rs10280394 |
|---|---|
| Chromosome Location | chr7:137767201-137767202 |
| allele | A/C |
| 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 | chr7:137745328..137748047-chr7:137765457..137767555,2 | K562 | blood: |
| No data |
| No data |
| No data |
| No data |
rSNPs within LD-proxies of this variant (count:22)
| rs_ID | r2[population] |
|---|---|
| rs10228704 | 0.80[AMR][1000 genomes] |
| rs10246884 | 0.98[EUR][1000 genomes];0.86[ASN][1000 genomes] |
| rs1025967 | 0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes] |
| rs10264658 | 0.95[AMR][1000 genomes];0.94[EUR][1000 genomes] |
| rs10280628 | 0.93[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
| rs10954602 | 0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];0.81[ASN][1000 genomes] |
| rs13243992 | 0.90[AMR][1000 genomes];0.94[EUR][1000 genomes] |
| rs1424379 | 0.83[ASN][1000 genomes] |
| rs1424380 | 0.85[ASN][1000 genomes] |
| rs2120846 | 0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];0.81[ASN][1000 genomes] |
| rs2166188 | 0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];0.81[ASN][1000 genomes] |
| rs2859828 | 0.96[EUR][1000 genomes];0.86[ASN][1000 genomes] |
| rs3757393 | 0.98[EUR][1000 genomes];0.84[ASN][1000 genomes] |
| rs3807332 | 0.98[EUR][1000 genomes];0.84[ASN][1000 genomes] |
| rs4732285 | 0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes] |
| rs6945659 | 0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes] |
| rs6954846 | 0.81[AMR][1000 genomes];0.87[ASN][1000 genomes] |
| rs6977075 | 0.95[AMR][1000 genomes];0.94[EUR][1000 genomes] |
| rs6980334 | 0.85[AMR][1000 genomes];0.89[EUR][1000 genomes] |
| rs7784881 | 0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes] |
| rs7787591 | 0.95[AMR][1000 genomes];0.94[EUR][1000 genomes] |
| rs7795946 | 0.93[AMR][1000 genomes];0.94[EUR][1000 genomes] |
Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page:
1
| No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
|---|---|---|---|---|---|---|---|
| 1 | nsv518070 | chr7:137534627-137808839 | Enhancers Flanking Active TSS Weak transcription Strong transcription Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNAmiRNA target site | 17 gene(s) | inside rSNPs | diseases |
| 2 | nsv831151 | chr7:137711447-137865471 | Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Active TSS Bivalent Enhancer Strong transcription Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA | 14 gene(s) | inside rSNPs | diseases |
| 3 | esv34048 | chr7:137724092-138213119 | Enhancers ZNF genes & repeats Flanking Active TSS Weak transcription Strong transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA | 35 gene(s) | inside rSNPs | diseases |
| 4 | nsv437032 | chr7:137753091-137773291 | Weak transcription Active TSS Enhancers Genic enhancers Flanking Active TSS ZNF genes & repeats | TF binding regionCpG islandChromatin interactive region | 4 gene(s) | inside rSNPs | diseases |
| No data |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr7:137767000-137767600 | Weak transcription | Liver | Liver |
