Variant report
Variant | rs62473831 |
---|---|
Chromosome Location | chr7:112260561-112260562 |
allele | G/T |
Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:2)
- LncRNA region (count:7)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
No data |
No data |
(count:2 , 50 per page) page:
1
(count:7 , 50 per page) page:
1
No. | lncRNA name | Chromosome Location | lncRNA alias |
---|---|---|---|
1 | lnc-C7orf53-2 | chr7:112260463-112260699 | XLOC_006210 |
2 | lnc-C7orf53-2 | chr7:112260463-112260814 | XLOC_006210 |
3 | lnc-C7orf53-2 | chr7:112260463-112260699 | XLOC_006210 |
4 | lnc-C7orf53-2 | chr7:112260463-112260698 | XLOC_006210 |
5 | lnc-C7orf53-2 | chr7:112260463-112260704 | NR_110159 |
6 | lnc-C7orf53-2 | chr7:112260463-112260704 | NR_110160 |
7 | lnc-C7orf53-2 | chr7:112260462-112260814 | NONHSAT122792 |
No data |
No data |
No data |
rs_ID | r2[population] |
---|---|
rs3128387 | 0.95[AMR][1000 genomes];0.80[EUR][1000 genomes] |
rs3128389 | 0.87[AMR][1000 genomes] |
rs43095 | 0.82[AFR][1000 genomes] |
rs62473829 | 0.83[EUR][1000 genomes] |
rs62473833 | 0.84[EUR][1000 genomes] |
rs73715656 | 0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv531436 | chr7:111856171-112585407 | Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 105 gene(s) | inside rSNPs | diseases |
2 | nsv889055 | chr7:112174089-112353440 | Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 8 gene(s) | inside rSNPs | diseases |
3 | nsv970931 | chr7:112259987-112260700 | Enhancers | Chromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
No data |