Variant report
Variant | rs17861376 |
---|---|
Chromosome Location | chr7:126592076-126592077 |
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] |
---|---|
rs1003036 | 0.96[CEU][hapmap] |
rs1121874 | 1.00[CEU][hapmap] |
rs1154324 | 1.00[CEU][hapmap] |
rs1154325 | 1.00[CEU][hapmap] |
rs1155597 | 1.00[CEU][hapmap] |
rs1204563 | 0.96[CEU][hapmap] |
rs1204567 | 0.96[CEU][hapmap] |
rs1204569 | 0.96[CEU][hapmap] |
rs1204579 | 0.96[CEU][hapmap] |
rs1204583 | 0.96[CEU][hapmap] |
rs1204588 | 1.00[CEU][hapmap] |
rs1204593 | 1.00[CEU][hapmap] |
rs1204594 | 1.00[CEU][hapmap] |
rs1211384 | 1.00[CEU][hapmap] |
rs1419465 | 0.96[CEU][hapmap] |
rs1548766 | 0.96[CEU][hapmap] |
rs2067052 | 0.96[CEU][hapmap] |
rs2072416 | 0.96[CEU][hapmap] |
rs2518949 | 0.96[CEU][hapmap] |
rs2518954 | 0.95[CEU][hapmap] |
rs2518955 | 0.96[CEU][hapmap] |
rs2535926 | 0.96[CEU][hapmap] |
rs2535932 | 0.96[CEU][hapmap] |
rs2535938 | 0.96[CEU][hapmap] |
rs6975379 | 1.00[CEU][hapmap] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | esv2758132 | chr7:126494789-126677843 | Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNA | 3 gene(s) | inside rSNPs | diseases |
2 | esv2759562 | chr7:126494789-126677843 | Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 3 gene(s) | inside rSNPs | diseases |
3 | nsv427805 | chr7:126494789-126677843 | Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNA | 3 gene(s) | inside rSNPs | diseases |
4 | nsv608378 | chr7:126570120-126597132 | Enhancers Weak transcription | Chromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
No data |