Variant report
Variant | rs72797914 |
---|---|
Chromosome Location | chr16:52072802-52072803 |
allele | A/G |
Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:0)
- LncRNA region (count:1)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
No data |
No data |
No data |
(count:1 , 50 per page) page:
1
No. | lncRNA name | Chromosome Location | lncRNA alias |
---|---|---|---|
1 | lnc-RP11-152O14.2.1-4 | chr16:52070371-52072963 | predAs_engstrom06_AK123139_1 |
No data |
No data |
No data |
rs_ID | r2[population] |
---|---|
rs1102396 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs1582316 | 0.81[ASN][1000 genomes] |
rs1582318 | 0.81[ASN][1000 genomes] |
rs1592481 | 0.81[ASN][1000 genomes] |
rs1600002 | 0.81[ASN][1000 genomes] |
rs1600003 | 0.81[ASN][1000 genomes] |
rs2059233 | 0.81[ASN][1000 genomes] |
rs2194291 | 0.98[EUR][1000 genomes];0.81[ASN][1000 genomes] |
rs256591 | 0.84[AMR][1000 genomes] |
rs33362 | 0.97[AFR][1000 genomes];0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.84[ASN][1000 genomes] |
rs33363 | 0.97[AFR][1000 genomes];0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes] |
rs33364 | 0.97[AFR][1000 genomes];0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes] |
rs42771 | 0.86[AMR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv492248 | chr16:51681902-52456082 | Enhancers Weak transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Active TSS Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 40 gene(s) | inside rSNPs | diseases |
2 | esv34024 | chr16:51878565-52316530 | Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNA | 33 gene(s) | inside rSNPs | diseases |
3 | nsv827650 | chr16:52067728-52124369 | Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 15 gene(s) | inside rSNPs | diseases |
No data |