Variant report
Variant | rs12436525 |
---|---|
Chromosome Location | chr14:84448559-84448560 |
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] |
---|---|
rs10484122 | 0.83[EUR][1000 genomes] |
rs11159625 | 0.81[EUR][1000 genomes] |
rs12433100 | 0.81[EUR][1000 genomes] |
rs12433667 | 0.90[ASN][1000 genomes] |
rs12434759 | 0.83[EUR][1000 genomes] |
rs12435187 | 0.81[EUR][1000 genomes] |
rs12435245 | 0.83[EUR][1000 genomes] |
rs12437234 | 0.94[ASN][1000 genomes] |
rs12586479 | 0.90[ASN][1000 genomes] |
rs12587115 | 0.96[ASN][1000 genomes] |
rs12587723 | 0.94[ASN][1000 genomes] |
rs12588733 | 0.90[ASN][1000 genomes] |
rs12588936 | 0.90[ASN][1000 genomes] |
rs12589845 | 0.90[ASN][1000 genomes] |
rs12590706 | 0.90[ASN][1000 genomes] |
rs12897738 | 0.83[EUR][1000 genomes] |
rs12898147 | 0.90[ASN][1000 genomes] |
rs17119417 | 0.90[ASN][1000 genomes] |
rs17119488 | 0.90[ASN][1000 genomes] |
rs17119542 | 0.87[ASN][1000 genomes] |
rs17647821 | 0.83[EUR][1000 genomes] |
rs17654374 | 0.81[EUR][1000 genomes] |
rs17726697 | 0.83[EUR][1000 genomes] |
rs1986658 | 0.96[ASN][1000 genomes] |
rs34708795 | 0.83[EUR][1000 genomes] |
rs4904149 | 0.90[ASN][1000 genomes] |
rs4904150 | 0.96[ASN][1000 genomes] |
rs4904154 | 0.87[ASN][1000 genomes] |
rs58445096 | 0.85[ASN][1000 genomes] |
rs61985922 | 0.81[EUR][1000 genomes] |
rs61985923 | 0.81[EUR][1000 genomes] |
rs61987170 | 0.82[EUR][1000 genomes] |
rs7157753 | 0.83[EUR][1000 genomes] |
rs72701041 | 0.90[ASN][1000 genomes] |
rs74069027 | 0.90[ASN][1000 genomes] |
rs8003423 | 0.83[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv1039271 | chr14:84405561-84467550 | Weak transcription Active TSS Enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer | Chromatin interactive region | n/a | inside rSNPs | n/a |
2 | nsv974291 | chr14:84447572-84460362 | Enhancers Weak transcription ZNF genes & repeats | Chromatin interactive region | n/a | inside rSNPs | n/a |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr14:84448400-84448600 | ZNF genes & repeats | Fetal Heart | heart |