Variant report
Variant | rs17061406 |
---|---|
Chromosome Location | chr6:101560373-101560374 |
allele | G/T |
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 |
rs_ID | r2[population] |
---|---|
rs10485425 | 0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs1149271 | 0.92[CHB][hapmap];0.84[JPT][hapmap];0.95[ASN][1000 genomes] |
rs12199600 | 0.95[ASN][1000 genomes] |
rs1342797 | 1.00[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs1342798 | 1.00[AFR][1000 genomes];1.00[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs1418713 | 1.00[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs17061234 | 0.92[CHB][hapmap];0.92[JPT][hapmap];0.84[ASN][1000 genomes] |
rs17061235 | 0.92[CHB][hapmap];0.92[JPT][hapmap];0.84[ASN][1000 genomes] |
rs17061236 | 0.84[ASN][1000 genomes] |
rs17061242 | 0.84[ASN][1000 genomes] |
rs17061360 | 1.00[AFR][1000 genomes];1.00[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs17061363 | 0.88[ASN][1000 genomes] |
rs17061371 | 1.00[EUR][1000 genomes];0.87[ASN][1000 genomes] |
rs17061413 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs17061496 | 0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs17061507 | 1.00[AFR][1000 genomes];1.00[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs17061509 | 1.00[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs17061513 | 0.88[ASN][1000 genomes] |
rs17061516 | 1.00[AFR][1000 genomes];1.00[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs17061520 | 1.00[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs17061525 | 1.00[AFR][1000 genomes];1.00[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs2180339 | 0.86[ASN][1000 genomes] |
rs2399728 | 1.00[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs3905201 | 1.00[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs4637650 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs648360 | 0.83[ASN][1000 genomes] |
rs705619 | 0.80[ASN][1000 genomes] |
rs73508859 | 0.84[ASN][1000 genomes] |
rs73760737 | 0.84[ASN][1000 genomes] |
rs73760738 | 0.84[ASN][1000 genomes] |
rs7451697 | 1.00[AFR][1000 genomes];1.00[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs768985 | 0.84[ASN][1000 genomes] |
rs9485429 | 0.84[ASN][1000 genomes] |
rs9498435 | 0.84[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv1020400 | chr6:101172705-101981665 | Weak transcription Bivalent/Poised TSS Enhancers Active TSS Strong transcription Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 10 gene(s) | inside rSNPs | diseases |
2 | nsv538390 | chr6:101172705-101981665 | Flanking Active TSS Weak transcription ZNF genes & repeats Enhancers Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 10 gene(s) | inside rSNPs | diseases |
3 | nsv1019213 | chr6:101225650-101623140 | Enhancers Flanking Active TSS Weak transcription Strong transcription Active TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 8 gene(s) | inside rSNPs | diseases |
4 | nsv538391 | chr6:101225650-101623140 | Active TSS Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Strong transcription Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 8 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr6:101549000-101563000 | Weak transcription | H1 BMP4 Derived Mesendoderm Cultured Cells | ES cell derived |
2 | chr6:101559200-101562200 | Weak transcription | ES-I3 Cell Line | embryonic stem cell |