Variant report
Variant | rs7819218 |
---|---|
Chromosome Location | chr8:63981226-63981227 |
allele | A/G |
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] |
---|---|
rs16930185 | 1.00[CEU][hapmap];0.88[EUR][1000 genomes] |
rs34766023 | 1.00[EUR][1000 genomes] |
rs55691782 | 0.88[EUR][1000 genomes] |
rs57520077 | 0.88[EUR][1000 genomes] |
rs58243916 | 0.88[EUR][1000 genomes] |
rs60596167 | 0.88[EUR][1000 genomes] |
rs60864225 | 0.88[EUR][1000 genomes] |
rs61402647 | 0.88[EUR][1000 genomes] |
rs6472070 | 1.00[CEU][hapmap] |
rs66507324 | 0.88[EUR][1000 genomes] |
rs66521539 | 0.88[EUR][1000 genomes] |
rs67530611 | 0.88[EUR][1000 genomes] |
rs67574340 | 0.88[EUR][1000 genomes] |
rs67833679 | 0.88[EUR][1000 genomes] |
rs67890556 | 0.88[EUR][1000 genomes] |
rs68126533 | 0.88[EUR][1000 genomes] |
rs6998706 | 0.91[YRI][hapmap] |
rs72655031 | 0.88[EUR][1000 genomes] |
rs72655032 | 0.88[EUR][1000 genomes] |
rs72655033 | 0.88[EUR][1000 genomes] |
rs72655040 | 0.88[EUR][1000 genomes] |
rs72655052 | 0.88[EUR][1000 genomes] |
rs72655076 | 0.88[EUR][1000 genomes] |
rs72656600 | 0.94[EUR][1000 genomes] |
rs72658335 | 0.94[EUR][1000 genomes] |
rs72658345 | 0.94[EUR][1000 genomes] |
rs72658355 | 0.94[EUR][1000 genomes] |
rs72658358 | 0.94[EUR][1000 genomes] |
rs72658363 | 1.00[EUR][1000 genomes] |
rs72658377 | 1.00[EUR][1000 genomes] |
rs72658378 | 1.00[EUR][1000 genomes] |
rs72658399 | 1.00[EUR][1000 genomes] |
rs72659805 | 1.00[EUR][1000 genomes] |
rs72659809 | 1.00[EUR][1000 genomes] |
rs72659816 | 0.89[EUR][1000 genomes] |
rs72659831 | 1.00[EUR][1000 genomes] |
rs72659834 | 1.00[EUR][1000 genomes] |
rs72659847 | 0.88[EUR][1000 genomes] |
rs72659848 | 0.88[EUR][1000 genomes] |
rs72659849 | 0.94[EUR][1000 genomes] |
rs72659850 | 0.88[EUR][1000 genomes] |
rs72659853 | 0.88[EUR][1000 genomes] |
rs72659855 | 0.94[EUR][1000 genomes] |
rs72659857 | 0.94[EUR][1000 genomes] |
rs72659859 | 0.94[EUR][1000 genomes] |
rs72659867 | 0.94[EUR][1000 genomes] |
rs72659879 | 0.88[EUR][1000 genomes] |
rs73272427 | 0.88[EUR][1000 genomes] |
rs73272436 | 0.88[EUR][1000 genomes] |
rs73272447 | 0.88[EUR][1000 genomes] |
rs7818582 | 0.91[YRI][hapmap] |
rs7818912 | 0.91[YRI][hapmap] |
rs7819204 | 0.91[YRI][hapmap] |
rs7821480 | 1.00[CEU][hapmap] |
rs7821895 | 1.00[CEU][hapmap];1.00[GIH][hapmap];1.00[MEX][hapmap] |
rs7843136 | 1.00[CEU][hapmap];1.00[GIH][hapmap] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv1033527 | chr8:63673915-64073735 | Active TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh Strong transcription Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 18 gene(s) | inside rSNPs | diseases |
2 | nsv465701 | chr8:63951237-64080486 | Weak transcription Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 14 gene(s) | inside rSNPs | diseases |
3 | nsv611448 | chr8:63951237-64080486 | Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer Transcr. at gene 5' and 3' Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 14 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr8:63971200-63984000 | Weak transcription | Foreskin Melanocyte Primary Cells skin03 | Skin |
2 | chr8:63977800-63989800 | Weak transcription | Foreskin Melanocyte Primary Cells skin01 | Skin |
3 | chr8:63979400-63984000 | Weak transcription | Aorta | Aorta |
4 | chr8:63979400-63984400 | Weak transcription | Placenta | Placenta |
5 | chr8:63980200-63981600 | Strong transcription | Liver | Liver |