Variant report
Variant | rs2654655 |
---|---|
Chromosome Location | chr12:61041194-61041195 |
allele | A/C |
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] |
---|---|
rs10082833 | 0.81[EUR][1000 genomes] |
rs10877452 | 0.80[EUR][1000 genomes] |
rs11173581 | 0.86[EUR][1000 genomes] |
rs11173625 | 0.81[EUR][1000 genomes] |
rs11173627 | 0.82[EUR][1000 genomes] |
rs12298398 | 0.85[EUR][1000 genomes] |
rs12301122 | 0.81[EUR][1000 genomes] |
rs12321112 | 0.90[EUR][1000 genomes] |
rs1353732 | 0.87[EUR][1000 genomes] |
rs1587345 | 0.82[EUR][1000 genomes] |
rs1604715 | 0.88[EUR][1000 genomes] |
rs273780 | 0.85[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes] |
rs273781 | 0.86[EUR][1000 genomes] |
rs273782 | 0.88[EUR][1000 genomes] |
rs273785 | 0.88[EUR][1000 genomes] |
rs273787 | 0.85[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes] |
rs4758883 | 0.84[EUR][1000 genomes] |
rs7134059 | 0.81[EUR][1000 genomes] |
rs7301607 | 0.82[EUR][1000 genomes] |
rs9669114 | 0.80[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv1047466 | chr12:60702221-61521156 | Active TSS Enhancers Weak transcription Bivalent/Poised TSS ZNF genes & repeats Flanking Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 8 gene(s) | inside rSNPs | diseases |
2 | nsv1051641 | chr12:60986661-61161174 | Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS | Chromatin interactive regionlncRNA | n/a | inside rSNPs | diseases |
3 | nsv541508 | chr12:60986661-61161174 | ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS | Chromatin interactive regionlncRNA | n/a | inside rSNPs | diseases |
4 | nsv1049626 | chr12:61005224-61095254 | Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS | Chromatin interactive regionlncRNA | n/a | inside rSNPs | diseases |
5 | nsv1035259 | chr12:61008196-61095254 | ZNF genes & repeats Enhancers Flanking Active TSS Weak transcription | Chromatin interactive regionlncRNA | n/a | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr12:61041000-61041200 | ZNF genes & repeats | ES-UCSF4 Cell Line | embryonic stem cell |