Variant report
Variant | rs60226 |
---|---|
Chromosome Location | chr8:85344643-85344644 |
allele | C/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] |
---|---|
rs10102848 | 0.80[JPT][hapmap] |
rs10112823 | 0.80[CEU][hapmap] |
rs12548307 | 0.81[JPT][hapmap] |
rs13261650 | 0.80[CEU][hapmap] |
rs13268314 | 0.85[JPT][hapmap] |
rs1388415 | 0.81[JPT][hapmap] |
rs1388416 | 0.81[JPT][hapmap] |
rs1491565 | 0.92[CEU][hapmap];1.00[JPT][hapmap] |
rs1491566 | 0.86[JPT][hapmap] |
rs1586798 | 0.81[JPT][hapmap] |
rs1907549 | 0.81[JPT][hapmap] |
rs2127220 | 1.00[CEU][hapmap];1.00[JPT][hapmap] |
rs317942 | 1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs317952 | 0.88[CEU][hapmap];0.88[GIH][hapmap] |
rs317954 | 0.88[CEU][hapmap];0.88[GIH][hapmap] |
rs4349980 | 0.86[JPT][hapmap] |
rs4504634 | 0.81[JPT][hapmap];0.82[TSI][hapmap] |
rs4639510 | 0.86[JPT][hapmap] |
rs4740009 | 0.86[JPT][hapmap] |
rs7000150 | 0.83[CEU][hapmap] |
rs7010963 | 0.86[JPT][hapmap] |
rs711009 | 0.80[CEU][hapmap];0.82[JPT][hapmap];0.81[AMR][1000 genomes];0.87[EUR][1000 genomes] |
rs711012 | 0.80[CEU][hapmap];0.82[JPT][hapmap];0.87[MEX][hapmap];0.85[EUR][1000 genomes] |
rs711014 | 0.80[CEU][hapmap];0.82[JPT][hapmap];0.87[MEX][hapmap];0.84[AMR][1000 genomes];0.86[EUR][1000 genomes] |
rs711017 | 0.80[CEU][hapmap];0.82[JPT][hapmap];0.84[AMR][1000 genomes];0.85[EUR][1000 genomes] |
rs711021 | 0.87[CEU][hapmap];0.82[JPT][hapmap] |
rs711026 | 0.80[CEU][hapmap];0.82[JPT][hapmap];0.81[AMR][1000 genomes];0.85[EUR][1000 genomes] |
rs711028 | 0.80[EUR][1000 genomes] |
rs711030 | 0.81[JPT][hapmap] |
rs711038 | 0.82[JPT][hapmap] |
rs711051 | 0.80[CEU][hapmap];0.82[JPT][hapmap];0.83[EUR][1000 genomes] |
rs7825684 | 0.86[JPT][hapmap] |
rs783787 | 0.80[CEU][hapmap] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv831375 | chr8:85272352-85463621 | Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS | Chromatin interactive region | n/a | inside rSNPs | diseases |
2 | esv3481417 | chr8:85279453-86145229 | Active TSS Weak transcription Flanking Active TSS Enhancers Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 29 gene(s) | inside rSNPs | diseases |
3 | esv3481418 | chr8:85279453-86145229 | Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 29 gene(s) | inside rSNPs | diseases |
4 | nsv1029152 | chr8:85292559-85352660 | Enhancers Weak transcription Active TSS | Chromatin interactive region | n/a | inside rSNPs | n/a |
No data |