Variant report
Variant | rs2180771 |
---|---|
Chromosome Location | chr6:82227770-82227771 |
allele | C/T |
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 |
---|---|
ENSG00000269494 | Chromatin interaction |
rs_ID | r2[population] |
---|---|
rs1321763 | 1.00[EUR][1000 genomes] |
rs1321764 | 1.00[EUR][1000 genomes] |
rs1341221 | 1.00[CEU][hapmap];1.00[EUR][1000 genomes] |
rs1341223 | 1.00[CEU][hapmap] |
rs16879669 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs16893157 | 1.00[EUR][1000 genomes] |
rs16893196 | 0.90[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs16893200 | 0.90[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs16893204 | 0.90[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs16893220 | 0.90[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs1853138 | 0.90[AMR][1000 genomes] |
rs1857302 | 1.00[EUR][1000 genomes] |
rs1923151 | 1.00[CEU][hapmap];1.00[EUR][1000 genomes] |
rs1923152 | 1.00[EUR][1000 genomes] |
rs1923153 | 1.00[EUR][1000 genomes] |
rs1923154 | 1.00[EUR][1000 genomes] |
rs2153644 | 1.00[CEU][hapmap];1.00[MEX][hapmap];1.00[EUR][1000 genomes] |
rs2185587 | 1.00[CEU][hapmap];1.00[EUR][1000 genomes] |
rs56139622 | 1.00[EUR][1000 genomes] |
rs56347700 | 1.00[EUR][1000 genomes] |
rs56354221 | 1.00[EUR][1000 genomes] |
rs57049010 | 1.00[EUR][1000 genomes] |
rs57540087 | 1.00[EUR][1000 genomes] |
rs58348892 | 1.00[EUR][1000 genomes] |
rs59561150 | 1.00[EUR][1000 genomes] |
rs59828216 | 1.00[EUR][1000 genomes] |
rs61279115 | 1.00[EUR][1000 genomes] |
rs6900056 | 1.00[CEU][hapmap];1.00[MEX][hapmap];1.00[EUR][1000 genomes] |
rs6903301 | 1.00[EUR][1000 genomes] |
rs6903470 | 1.00[EUR][1000 genomes] |
rs6903966 | 1.00[EUR][1000 genomes] |
rs6904093 | 1.00[EUR][1000 genomes] |
rs6904760 | 1.00[EUR][1000 genomes] |
rs6905459 | 1.00[CEU][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs6907542 | 0.90[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs6909563 | 1.00[EUR][1000 genomes] |
rs6915424 | 1.00[EUR][1000 genomes] |
rs6923049 | 1.00[EUR][1000 genomes] |
rs6923636 | 1.00[EUR][1000 genomes] |
rs6926893 | 1.00[EUR][1000 genomes] |
rs6931780 | 1.00[EUR][1000 genomes] |
rs6932354 | 1.00[EUR][1000 genomes] |
rs6935793 | 1.00[EUR][1000 genomes] |
rs73749103 | 1.00[EUR][1000 genomes] |
rs73749105 | 1.00[EUR][1000 genomes] |
rs73749107 | 1.00[EUR][1000 genomes] |
rs73749108 | 1.00[EUR][1000 genomes] |
rs73749122 | 1.00[EUR][1000 genomes] |
rs73749125 | 1.00[EUR][1000 genomes] |
rs73749126 | 1.00[EUR][1000 genomes] |
rs73749127 | 1.00[EUR][1000 genomes] |
rs73749128 | 1.00[EUR][1000 genomes] |
rs73749130 | 1.00[EUR][1000 genomes] |
rs73749131 | 1.00[EUR][1000 genomes] |
rs73749132 | 1.00[EUR][1000 genomes] |
rs73749134 | 1.00[EUR][1000 genomes] |
rs73749135 | 1.00[EUR][1000 genomes] |
rs73749136 | 1.00[EUR][1000 genomes] |
rs73749137 | 1.00[EUR][1000 genomes] |
rs73749138 | 1.00[EUR][1000 genomes] |
rs73749139 | 1.00[EUR][1000 genomes] |
rs73749140 | 1.00[EUR][1000 genomes] |
rs73749141 | 1.00[EUR][1000 genomes] |
rs73749142 | 1.00[EUR][1000 genomes] |
rs73749183 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs73751432 | 1.00[EUR][1000 genomes] |
rs73751433 | 1.00[EUR][1000 genomes] |
rs73751439 | 1.00[EUR][1000 genomes] |
rs73751440 | 1.00[EUR][1000 genomes] |
rs73751441 | 1.00[EUR][1000 genomes] |
rs73751443 | 1.00[EUR][1000 genomes] |
rs73751445 | 1.00[EUR][1000 genomes] |
rs7739429 | 1.00[EUR][1000 genomes] |
rs9688608 | 1.00[CEU][hapmap];1.00[EUR][1000 genomes] |
rs9688618 | 1.00[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv604087 | chr6:81792413-82326091 | Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 4 gene(s) | inside rSNPs | diseases |
No data |