Variant report
Variant | rs73443517 |
---|---|
Chromosome Location | chr7:136470589-136470590 |
allele | C/T |
Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:0)
- LncRNA region (count:3)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
No data |
No data |
No data |
(count:3 , 50 per page) page:
1
No. | lncRNA name | Chromosome Location | lncRNA alias |
---|---|---|---|
1 | lnc-PTN-2 | chr7:136468822-136470638 | ENSG00000234352 |
2 | lnc-PTN-2 | chr7:136470446-136470638 | ENSG00000234352.5 |
3 | lnc-PTN-2 | chr7:136470446-136470638 | ENSG00000234352.5 |
No data |
No data |
No data |
rs_ID | r2[population] |
---|---|
rs58692102 | 0.93[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs59103221 | 1.00[AMR][1000 genomes] |
rs59580970 | 1.00[AMR][1000 genomes] |
rs61093667 | 1.00[AMR][1000 genomes] |
rs73443599 | 1.00[AMR][1000 genomes] |
rs73445249 | 1.00[AMR][1000 genomes] |
rs73457645 | 1.00[AMR][1000 genomes] |
rs73459634 | 1.00[AMR][1000 genomes] |
rs73459657 | 1.00[AMR][1000 genomes] |
rs73459662 | 1.00[AMR][1000 genomes] |
rs73459663 | 1.00[AMR][1000 genomes] |
rs73459665 | 1.00[AMR][1000 genomes] |
rs73459667 | 1.00[AMR][1000 genomes] |
rs73459677 | 1.00[AMR][1000 genomes] |
rs73459684 | 1.00[AMR][1000 genomes] |
rs73459697 | 1.00[AMR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | esv3374876 | chr7:136413245-136480051 | Enhancers Weak transcription Active TSS | Chromatin interactive regionlncRNA | 1 gene(s) | inside rSNPs | diseases |
2 | nsv1029192 | chr7:136433278-137147566 | Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNAmiRNA target site | 23 gene(s) | inside rSNPs | diseases |
No data |