Variant report
Variant | rs10103138 |
---|---|
Chromosome Location | chr8:91441070-91441071 |
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] |
---|---|
rs10086788 | 0.90[AMR][1000 genomes];0.89[EUR][1000 genomes] |
rs10087100 | 0.96[EUR][1000 genomes] |
rs10099647 | 0.90[AMR][1000 genomes];0.89[EUR][1000 genomes] |
rs10100832 | 0.81[EUR][1000 genomes] |
rs10100923 | 0.92[EUR][1000 genomes] |
rs10103125 | 0.90[AMR][1000 genomes];0.89[EUR][1000 genomes] |
rs10103492 | 1.00[CEU][hapmap] |
rs10104445 | 0.95[AMR][1000 genomes];0.96[EUR][1000 genomes] |
rs10104451 | 0.85[AMR][1000 genomes];0.89[EUR][1000 genomes] |
rs10106274 | 0.96[EUR][1000 genomes] |
rs10111531 | 0.85[AMR][1000 genomes];0.89[EUR][1000 genomes] |
rs10112375 | 0.96[EUR][1000 genomes] |
rs10112676 | 0.90[AMR][1000 genomes];0.89[EUR][1000 genomes] |
rs10156381 | 0.87[EUR][1000 genomes] |
rs1015844 | 0.96[EUR][1000 genomes] |
rs10216873 | 0.89[EUR][1000 genomes] |
rs11995911 | 1.00[CEU][hapmap] |
rs11996705 | 1.00[CEU][hapmap] |
rs11997568 | 0.83[EUR][1000 genomes] |
rs13439871 | 0.96[EUR][1000 genomes] |
rs16904545 | 1.00[EUR][1000 genomes] |
rs16904875 | 1.00[CEU][hapmap] |
rs16904876 | 1.00[CEU][hapmap] |
rs28385552 | 0.92[EUR][1000 genomes] |
rs28550265 | 0.96[EUR][1000 genomes] |
rs28610968 | 0.87[EUR][1000 genomes] |
rs28684622 | 0.96[EUR][1000 genomes] |
rs28882092 | 0.96[EUR][1000 genomes] |
rs4474067 | 0.90[AMR][1000 genomes];0.83[EUR][1000 genomes] |
rs4570116 | 1.00[CEU][hapmap] |
rs5005584 | 1.00[CEU][hapmap] |
rs58836045 | 0.90[AMR][1000 genomes];0.89[EUR][1000 genomes] |
rs9297838 | 0.96[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv981884 | chr8:91420804-91441125 | Enhancers Weak transcription | Chromatin interactive regionlncRNA | n/a | inside rSNPs | n/a |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr8:91441000-91445800 | Weak transcription | ES-I3 Cell Line | embryonic stem cell |