Variant report
Variant | rs10046419 |
---|---|
Chromosome Location | chr6:28007930-28007931 |
allele | A/C |
Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:2)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
No data |
No data |
(count:2 , 50 per page) page:
1
No data |
No data |
No data |
Variant related genes | Relation type |
---|---|
ENSG00000196331 | Chromatin interaction |
ENSG00000197153 | Chromatin interaction |
ENSG00000233224 | Chromatin interaction |
ENSG00000197914 | Chromatin interaction |
rs_ID | r2[population] |
---|---|
rs10046424 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs12178430 | 0.83[ASN][1000 genomes] |
rs12332927 | 0.82[CHB][hapmap] |
rs12333142 | 0.91[ASN][1000 genomes] |
rs1497525 | 1.00[CEU][hapmap];1.00[CHB][hapmap];0.81[JPT][hapmap];0.87[ASN][1000 genomes] |
rs1497526 | 1.00[CHB][hapmap];0.81[ASN][1000 genomes] |
rs1564442 | 1.00[CHB][hapmap] |
rs16893533 | 1.00[CEU][hapmap];1.00[CHB][hapmap];0.83[YRI][hapmap];0.83[ASN][1000 genomes] |
rs16893540 | 1.00[CEU][hapmap];1.00[CHB][hapmap];0.89[YRI][hapmap];0.91[ASN][1000 genomes] |
rs16893549 | 0.91[ASN][1000 genomes] |
rs16893731 | 1.00[CHB][hapmap] |
rs16893801 | 1.00[CHB][hapmap] |
rs17763319 | 1.00[CEU][hapmap];1.00[CHB][hapmap] |
rs17765402 | 1.00[CEU][hapmap];1.00[CHB][hapmap] |
rs17767294 | 1.00[CHB][hapmap] |
rs1873213 | 1.00[CHB][hapmap];0.89[ASN][1000 genomes] |
rs2277103 | 1.00[CHB][hapmap] |
rs2299030 | 0.82[CHB][hapmap] |
rs3757186 | 1.00[CHB][hapmap] |
rs6456803 | 1.00[CEU][hapmap];0.82[CHB][hapmap] |
rs73386659 | 0.83[ASN][1000 genomes] |
rs73392694 | 0.83[ASN][1000 genomes] |
rs73394718 | 0.81[ASN][1000 genomes] |
rs7760871 | 1.00[CEU][hapmap];1.00[CHB][hapmap];0.83[YRI][hapmap];0.83[ASN][1000 genomes] |
rs9461420 | 0.87[ASN][1000 genomes] |
rs9461424 | 1.00[CHB][hapmap];0.81[JPT][hapmap] |
rs9461425 | 1.00[CHB][hapmap] |
rs9468252 | 0.82[CHB][hapmap];0.83[ASN][1000 genomes] |
rs9468254 | 1.00[CEU][hapmap];1.00[CHB][hapmap];0.87[ASN][1000 genomes] |
rs9468264 | 1.00[CEU][hapmap];1.00[CHB][hapmap];0.81[JPT][hapmap];0.84[YRI][hapmap] |
rs9885649 | 0.82[CHB][hapmap];0.81[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv432858 | chr6:27719375-28011652 | Flanking Active TSS Weak transcription Enhancers Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 387 gene(s) | inside rSNPs | diseases |
2 | nsv1022651 | chr6:27864217-28017997 | Flanking Active TSS Enhancers Bivalent/Poised TSS Active TSS Weak transcription Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 50 gene(s) | inside rSNPs | diseases |
3 | nsv830619 | chr6:27872302-28062544 | Active TSS ZNF genes & repeats Enhancers Flanking Active TSS Weak transcription Strong transcription Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 38 gene(s) | inside rSNPs | diseases |
4 | nsv883513 | chr6:27982152-28033087 | Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 12 gene(s) | inside rSNPs | diseases |
5 | nsv981052 | chr6:27987196-28024382 | Bivalent Enhancer | TF binding regionCpG islandChromatin interactive region | 12 gene(s) | inside rSNPs | diseases |
No data |