Variant report
Variant | rs73316572 |
---|---|
Chromosome Location | chr7:19073759-19073760 |
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] |
---|---|
rs1016981 | 1.00[EUR][1000 genomes] |
rs1029435 | 1.00[ASN][1000 genomes] |
rs11973490 | 1.00[ASN][1000 genomes] |
rs11975429 | 1.00[ASN][1000 genomes] |
rs11982017 | 1.00[ASN][1000 genomes] |
rs11982021 | 1.00[ASN][1000 genomes] |
rs1468178 | 1.00[EUR][1000 genomes] |
rs17140572 | 1.00[EUR][1000 genomes] |
rs17140626 | 1.00[EUR][1000 genomes] |
rs2011513 | 1.00[EUR][1000 genomes] |
rs2097710 | 1.00[EUR][1000 genomes] |
rs2106723 | 1.00[EUR][1000 genomes] |
rs2214209 | 1.00[EUR][1000 genomes] |
rs2214313 | 1.00[ASN][1000 genomes] |
rs2263234 | 1.00[EUR][1000 genomes] |
rs2428348 | 1.00[EUR][1000 genomes] |
rs2521724 | 1.00[EUR][1000 genomes] |
rs2521725 | 0.89[EUR][1000 genomes] |
rs2521726 | 1.00[EUR][1000 genomes] |
rs2521727 | 1.00[EUR][1000 genomes] |
rs2521728 | 1.00[EUR][1000 genomes] |
rs2521730 | 1.00[EUR][1000 genomes] |
rs2521731 | 1.00[EUR][1000 genomes] |
rs2521736 | 1.00[EUR][1000 genomes] |
rs2717326 | 1.00[EUR][1000 genomes] |
rs2717335 | 1.00[EUR][1000 genomes] |
rs2717336 | 1.00[EUR][1000 genomes] |
rs2717341 | 1.00[EUR][1000 genomes] |
rs2717366 | 1.00[EUR][1000 genomes] |
rs58479714 | 1.00[ASN][1000 genomes] |
rs59296569 | 1.00[ASN][1000 genomes] |
rs60603722 | 1.00[ASN][1000 genomes] |
rs6966480 | 1.00[ASN][1000 genomes] |
rs6970356 | 1.00[ASN][1000 genomes] |
rs73314889 | 1.00[ASN][1000 genomes] |
rs73314898 | 1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs73314902 | 1.00[ASN][1000 genomes] |
rs73316504 | 1.00[ASN][1000 genomes] |
rs73323560 | 1.00[EUR][1000 genomes] |
rs886226 | 0.90[AFR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs886228 | 1.00[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv531020 | chr7:18971153-19261019 | Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 8 gene(s) | inside rSNPs | diseases |
2 | nsv887817 | chr7:19021592-19100076 | Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Active TSS | Chromatin interactive regionlncRNA | 1 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr7:19064400-19084800 | Weak transcription | Foreskin Fibroblast Primary Cells skin01 | Skin |
2 | chr7:19064400-19084800 | Weak transcription | Foreskin Fibroblast Primary Cells skin02 | Skin |
3 | chr7:19070400-19082200 | Weak transcription | HSMM | muscle |
4 | chr7:19071600-19081400 | Weak transcription | NHDF-Ad | bronchial |