Variant report
Variant | rs10094028 |
---|---|
Chromosome Location | chr8:122886795-122886796 |
allele | A/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] |
---|---|
rs10086515 | 1.00[ASN][1000 genomes] |
rs10086612 | 1.00[ASN][1000 genomes] |
rs10094891 | 0.81[EUR][1000 genomes];0.86[ASN][1000 genomes] |
rs10095392 | 0.88[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs10101375 | 1.00[ASN][1000 genomes] |
rs10101403 | 0.94[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs10101470 | 1.00[ASN][1000 genomes] |
rs10104333 | 0.88[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs10104809 | 1.00[ASN][1000 genomes] |
rs10105318 | 1.00[ASN][1000 genomes] |
rs10108701 | 0.94[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs10108705 | 1.00[ASN][1000 genomes] |
rs10110100 | 1.00[ASN][1000 genomes] |
rs10110106 | 0.88[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs10110134 | 0.88[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs10110297 | 0.88[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs1030977 | 0.86[ASN][1000 genomes] |
rs1030978 | 0.86[ASN][1000 genomes] |
rs1030979 | 0.86[ASN][1000 genomes] |
rs10956058 | 1.00[ASN][1000 genomes] |
rs10956062 | 1.00[ASN][1000 genomes] |
rs11781753 | 0.86[ASN][1000 genomes] |
rs11990026 | 1.00[ASN][1000 genomes] |
rs12676842 | 1.00[ASN][1000 genomes] |
rs13251152 | 1.00[ASN][1000 genomes] |
rs13251300 | 0.86[ASN][1000 genomes] |
rs13261004 | 0.88[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs13263521 | 0.88[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs1371715 | 0.86[ASN][1000 genomes] |
rs1371716 | 0.86[ASN][1000 genomes] |
rs1371717 | 0.86[ASN][1000 genomes] |
rs1371718 | 0.86[ASN][1000 genomes] |
rs1371719 | 0.86[ASN][1000 genomes] |
rs4128641 | 1.00[ASN][1000 genomes] |
rs4242327 | 1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes] |
rs4242328 | 1.00[ASN][1000 genomes] |
rs4268133 | 0.88[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs4317573 | 0.88[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs4327868 | 0.88[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs4413781 | 1.00[ASN][1000 genomes] |
rs4431601 | 1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs4433151 | 0.88[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs4464973 | 0.88[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs4518675 | 0.88[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs4520174 | 0.88[EUR][1000 genomes] |
rs4529469 | 0.88[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs4537307 | 1.00[ASN][1000 genomes] |
rs4567046 | 0.88[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs4582571 | 0.88[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs4582572 | 0.88[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs4609198 | 0.88[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs4641072 | 0.88[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs4871212 | 0.88[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs6470041 | 0.86[ASN][1000 genomes] |
rs6470047 | 1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs6984179 | 0.94[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs6999640 | 1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes] |
rs6999793 | 1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes] |
rs7001379 | 1.00[ASN][1000 genomes] |
rs7001394 | 1.00[ASN][1000 genomes] |
rs7001741 | 1.00[ASN][1000 genomes] |
rs7002399 | 1.00[ASN][1000 genomes] |
rs7002779 | 1.00[ASN][1000 genomes] |
rs7003107 | 1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs7003690 | 0.86[ASN][1000 genomes] |
rs7003896 | 0.88[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs7004948 | 1.00[ASN][1000 genomes] |
rs7009055 | 1.00[ASN][1000 genomes] |
rs7012540 | 1.00[CHB][hapmap] |
rs7822873 | 0.94[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs9297655 | 0.94[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs964868 | 0.86[ASN][1000 genomes] |
rs964869 | 0.86[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | esv2752207 | chr8:122869651-122961848 | Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNA | 3 gene(s) | inside rSNPs | n/a |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr8:122881800-122896800 | Weak transcription | H1 BMP4 Derived Mesendoderm Cultured Cells | ES cell derived |