Variant report
| Variant | rs7801079 |
|---|---|
| Chromosome Location | chr7:104284692-104284693 |
| allele | A/G |
| Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:3)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
| No data |
| No data |
(count:3 , 50 per page) page:
1
| No data |
| No data |
| No data |
| No data |
| rs_ID | r2[population] |
|---|---|
| rs10250078 | 1.00[AMR][1000 genomes] |
| rs10270888 | 0.83[YRI][hapmap] |
| rs10271797 | 1.00[YRI][hapmap] |
| rs10272959 | 0.82[YRI][hapmap] |
| rs12705235 | 0.82[YRI][hapmap] |
| rs1465342 | 1.00[YRI][hapmap];0.91[AFR][1000 genomes] |
| rs1468861 | 1.00[AMR][1000 genomes] |
| rs1468864 | 1.00[YRI][hapmap];0.87[AFR][1000 genomes] |
| rs1548938 | 0.82[YRI][hapmap] |
| rs1861610 | 1.00[AMR][1000 genomes] |
| rs2008042 | 0.87[AFR][1000 genomes] |
| rs2080483 | 1.00[YRI][hapmap] |
| rs2193198 | 1.00[YRI][hapmap] |
| rs2193199 | 1.00[YRI][hapmap];0.86[AFR][1000 genomes];1.00[AMR][1000 genomes] |
| rs2193200 | 1.00[YRI][hapmap] |
| rs2385238 | 0.83[YRI][hapmap] |
| rs2385251 | 1.00[YRI][hapmap] |
| rs2385254 | 1.00[YRI][hapmap];0.87[AFR][1000 genomes] |
| rs2470962 | 1.00[AMR][1000 genomes] |
| rs4431535 | 1.00[AMR][1000 genomes] |
| rs4623345 | 1.00[AMR][1000 genomes] |
| rs4730033 | 0.98[AFR][1000 genomes];1.00[AMR][1000 genomes] |
| rs4730046 | 1.00[AMR][1000 genomes] |
| rs6944590 | 1.00[YRI][hapmap];0.98[AFR][1000 genomes];1.00[AMR][1000 genomes] |
| rs6958342 | 1.00[AMR][1000 genomes] |
| rs6960459 | 0.86[AFR][1000 genomes] |
| rs7784639 | 1.00[YRI][hapmap];0.98[AFR][1000 genomes];1.00[AMR][1000 genomes] |
| rs7801340 | 1.00[YRI][hapmap];0.98[AFR][1000 genomes];1.00[AMR][1000 genomes] |
Variant overlapped rSNPs/rCNVs (count:1 , 50 per page) page:
1
| No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
|---|---|---|---|---|---|---|---|
| 1 | nsv1024532 | chr7:104281393-104299847 | Enhancers Bivalent Enhancer Active TSS Weak transcription Flanking Active TSS | Chromatin interactive region | n/a | inside rSNPs | diseases |
| No data |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr7:104283200-104284800 | Enhancers | Foreskin Melanocyte Primary Cells skin03 | Skin |
| 2 | chr7:104284200-104285000 | Enhancers | Ganglion Eminence derived primary cultured neurospheres | brain |





