Variant report
Variant | rs12210224 |
---|---|
Chromosome Location | chr6:91976225-91976226 |
allele | A/G |
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] |
---|---|
rs10498972 | 0.88[EUR][1000 genomes] |
rs10755495 | 0.81[ASN][1000 genomes] |
rs12213909 | 1.00[AFR][1000 genomes];0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs13199295 | 0.83[ASN][1000 genomes] |
rs2069205 | 0.86[ASN][1000 genomes] |
rs2655645 | 0.90[ASN][1000 genomes] |
rs2748282 | 0.88[AFR][1000 genomes];0.91[ASN][1000 genomes] |
rs34506966 | 0.82[ASN][1000 genomes] |
rs4314472 | 0.82[ASN][1000 genomes] |
rs4376328 | 0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs4376329 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs4380725 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs4382224 | 0.81[ASN][1000 genomes] |
rs4391241 | 0.82[ASN][1000 genomes] |
rs4434442 | 0.83[ASN][1000 genomes] |
rs4473838 | 0.82[ASN][1000 genomes] |
rs4510643 | 0.82[ASN][1000 genomes] |
rs4513761 | 1.00[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs4707663 | 0.82[ASN][1000 genomes] |
rs4707667 | 0.81[ASN][1000 genomes] |
rs4707668 | 0.81[ASN][1000 genomes] |
rs4707670 | 0.81[ASN][1000 genomes] |
rs62417891 | 0.81[EUR][1000 genomes] |
rs6454848 | 0.82[ASN][1000 genomes] |
rs6454850 | 0.81[ASN][1000 genomes] |
rs6907539 | 0.88[EUR][1000 genomes] |
rs6916809 | 0.84[ASN][1000 genomes] |
rs6917281 | 0.84[ASN][1000 genomes] |
rs7740461 | 0.85[ASN][1000 genomes] |
rs7758710 | 0.85[ASN][1000 genomes] |
rs7759032 | 0.85[ASN][1000 genomes] |
rs9294485 | 0.81[ASN][1000 genomes] |
rs9345114 | 0.89[EUR][1000 genomes] |
rs9345121 | 0.83[ASN][1000 genomes] |
rs9353810 | 0.89[EUR][1000 genomes] |
rs9353811 | 0.89[EUR][1000 genomes] |
rs9353815 | 0.91[AFR][1000 genomes];0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs9359934 | 0.82[ASN][1000 genomes] |
rs9362858 | 0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes] |
rs9362864 | 0.82[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | esv2752130 | chr6:91740447-92196479 | Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 7 gene(s) | inside rSNPs | diseases |
2 | nsv1031681 | chr6:91784557-92075312 | Flanking Bivalent TSS/Enh Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS | Chromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
3 | nsv538359 | chr6:91784557-92075312 | Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS | Chromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
4 | nsv1017467 | chr6:91802015-92417554 | Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA | 12 gene(s) | inside rSNPs | diseases |
5 | nsv538360 | chr6:91802015-92417554 | Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA | 12 gene(s) | inside rSNPs | diseases |
6 | esv2422475 | chr6:91818508-91998748 | Weak transcription Enhancers Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Active TSS | Chromatin interactive region | n/a | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr6:91975200-91978400 | Weak transcription | Fetal Adrenal Gland | Adrenal Gland |
2 | chr6:91976200-91978400 | Enhancers | Fetal Lung | lung |