Variant report
Variant | rs11003908 |
---|---|
Chromosome Location | chr10:55645842-55645843 |
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] |
---|---|
rs10763016 | 0.95[CHB][hapmap];1.00[JPT][hapmap] |
rs10825123 | 0.83[GIH][hapmap] |
rs10825147 | 0.95[CHB][hapmap];1.00[JPT][hapmap] |
rs10825148 | 0.95[CHB][hapmap];1.00[JPT][hapmap] |
rs10825149 | 0.90[CHB][hapmap];1.00[JPT][hapmap];0.92[YRI][hapmap] |
rs10825154 | 0.94[JPT][hapmap] |
rs10825168 | 0.90[CHB][hapmap];0.82[CHD][hapmap];0.94[GIH][hapmap];0.94[JPT][hapmap] |
rs11003873 | 0.83[GIH][hapmap] |
rs11003894 | 1.00[CEU][hapmap] |
rs11003901 | 0.86[MKK][hapmap] |
rs11003902 | 0.84[CHB][hapmap] |
rs11003909 | 0.86[AFR][1000 genomes] |
rs11003916 | 1.00[CEU][hapmap];1.00[GIH][hapmap] |
rs11003921 | 1.00[CEU][hapmap];1.00[EUR][1000 genomes] |
rs11003924 | 0.88[JPT][hapmap] |
rs11003925 | 0.88[JPT][hapmap] |
rs11003927 | 0.95[CHB][hapmap];0.88[CHD][hapmap];0.94[GIH][hapmap];0.94[JPT][hapmap] |
rs12218632 | 0.86[YRI][hapmap] |
rs12572470 | 0.84[GIH][hapmap] |
rs16937793 | 0.88[GIH][hapmap] |
rs16937801 | 1.00[CEU][hapmap] |
rs16937805 | 0.85[MKK][hapmap] |
rs16937813 | 1.00[CEU][hapmap];1.00[GIH][hapmap];1.00[EUR][1000 genomes] |
rs16937840 | 0.90[CHB][hapmap];0.94[JPT][hapmap] |
rs1900414 | 0.88[JPT][hapmap] |
rs1900425 | 0.95[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap] |
rs1900426 | 0.88[CHB][hapmap] |
rs1900427 | 0.95[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap] |
rs1911427 | 0.81[CHB][hapmap];0.88[JPT][hapmap] |
rs2069215 | 1.00[CEU][hapmap];1.00[EUR][1000 genomes] |
rs2069216 | 0.99[ASN][1000 genomes] |
rs2069217 | 1.00[CEU][hapmap];1.00[CHB][hapmap];0.94[JPT][hapmap];0.93[YRI][hapmap];0.95[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs2593126 | 0.83[JPT][hapmap] |
rs2610822 | 0.81[ASW][hapmap];0.83[MKK][hapmap] |
rs2610846 | 0.90[CHB][hapmap];0.94[JPT][hapmap] |
rs2921922 | 0.86[JPT][hapmap] |
rs2921923 | 0.82[JPT][hapmap] |
rs2926390 | 0.82[MKK][hapmap] |
rs2926411 | 0.88[JPT][hapmap] |
rs41487044 | 0.95[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs4287256 | 0.83[CHB][hapmap] |
rs4364970 | 0.83[CHB][hapmap] |
rs4466737 | 0.83[CHB][hapmap] |
rs4478892 | 0.95[CHB][hapmap];0.97[CHD][hapmap];1.00[JPT][hapmap] |
rs4488106 | 0.84[JPT][hapmap] |
rs4586053 | 0.84[CHB][hapmap] |
rs7067725 | 0.83[JPT][hapmap] |
rs7083009 | 0.95[CHB][hapmap];1.00[JPT][hapmap] |
rs73246867 | 0.89[EUR][1000 genomes] |
rs7898068 | 0.88[JPT][hapmap] |
rs7905665 | 0.95[CHB][hapmap];1.00[JPT][hapmap] |
rs7905801 | 0.95[CHB][hapmap];1.00[JPT][hapmap] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | esv1842975 | chr10:55378668-55736655 | ZNF genes & repeats Enhancers Active TSS Weak transcription Flanking Active TSS Strong transcription Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 4 gene(s) | inside rSNPs | diseases |
2 | nsv949692 | chr10:55502542-55893206 | Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Bivalent/Poised TSS Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 4 gene(s) | inside rSNPs | diseases |
3 | nsv895429 | chr10:55564355-55736655 | Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Active TSS Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
4 | nsv550947 | chr10:55634290-55662226 | Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent/Poised TSS | Chromatin interactive region | n/a | inside rSNPs | diseases |
5 | nsv1049442 | chr10:55638740-55681002 | Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Active TSS | TF binding regionCpG islandChromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr10:55645800-55646600 | Enhancers | Liver | Liver |