Variant report
Variant | rs9370383 |
---|---|
Chromosome Location | chr6:54981216-54981217 |
allele | C/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] |
---|---|
rs12175211 | 1.00[CHB][hapmap] |
rs13211183 | 1.00[GIH][hapmap] |
rs35576476 | 1.00[EUR][1000 genomes] |
rs4518485 | 0.91[AFR][1000 genomes];0.84[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes] |
rs4594937 | 1.00[EUR][1000 genomes] |
rs62416376 | 0.84[ASN][1000 genomes] |
rs62416415 | 0.90[ASN][1000 genomes] |
rs62416457 | 0.90[ASN][1000 genomes] |
rs6937662 | 0.91[AFR][1000 genomes];0.84[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes] |
rs71560884 | 0.81[EUR][1000 genomes] |
rs9349746 | 1.00[EUR][1000 genomes] |
rs9357827 | 1.00[EUR][1000 genomes] |
rs9357830 | 1.00[EUR][1000 genomes] |
rs9367613 | 1.00[CHB][hapmap];1.00[JPT][hapmap];0.90[ASN][1000 genomes] |
rs9370339 | 1.00[CHB][hapmap];0.85[JPT][hapmap] |
rs9370340 | 1.00[CHB][hapmap];1.00[CHD][hapmap];0.85[JPT][hapmap] |
rs9370349 | 0.81[EUR][1000 genomes] |
rs9370365 | 1.00[EUR][1000 genomes] |
rs9370376 | 0.84[ASN][1000 genomes] |
rs9382401 | 1.00[CHB][hapmap];0.85[JPT][hapmap] |
rs9382423 | 1.00[EUR][1000 genomes] |
rs9382424 | 1.00[EUR][1000 genomes] |
rs9382425 | 0.88[EUR][1000 genomes] |
rs9382439 | 0.84[ASN][1000 genomes] |
rs9382451 | 0.90[ASN][1000 genomes] |
rs9382453 | 0.82[ASN][1000 genomes] |
rs9396029 | 1.00[EUR][1000 genomes] |
rs9396030 | 1.00[EUR][1000 genomes] |
rs9396037 | 1.00[CHB][hapmap] |
rs9396048 | 0.90[ASN][1000 genomes] |
rs9396049 | 0.90[ASN][1000 genomes] |
rs9637955 | 0.90[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv1033543 | chr6:54978528-55000338 | Enhancers Weak transcription | Chromatin interactive region | n/a | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr6:54980400-54981600 | Weak transcription | Duodenum Mucosa | Duodenum |