Variant report

Variant	rs10195342
Chromosome Location	chr2:211285730-211285731
allele	A/C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 55 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:52)

rs_ID	r²[population]
rs1027901	0.85[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1044708	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10804181	0.85[AMR][1000 genomes];0.92[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10804182	0.85[EUR][1000 genomes]
rs10804183	0.85[EUR][1000 genomes]
rs11889228	0.85[EUR][1000 genomes]
rs11894867	0.85[AMR][1000 genomes];0.89[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs11896108	0.85[AMR][1000 genomes];0.90[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs11900468	0.86[AMR][1000 genomes];0.89[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12469589	0.85[AMR][1000 genomes];0.94[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12473150	0.86[AMR][1000 genomes];0.88[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs12477237	0.81[EUR][1000 genomes]
rs1350463	0.83[AMR][1000 genomes];0.89[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1379838	0.85[AMR][1000 genomes];0.91[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1812875	0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2021214	0.85[AMR][1000 genomes];0.92[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2287424	0.84[EUR][1000 genomes]
rs2287425	0.85[EUR][1000 genomes]
rs2287429	0.86[EUR][1000 genomes]
rs2287430	0.86[EUR][1000 genomes]
rs2287432	0.86[EUR][1000 genomes]
rs2287433	0.80[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs2370949	0.85[EUR][1000 genomes]
rs2370956	0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2887899	0.86[EUR][1000 genomes]
rs35314871	0.83[AMR][1000 genomes];0.93[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs3755184	0.88[EUR][1000 genomes]
rs3770689	0.86[EUR][1000 genomes]
rs3770694	0.85[EUR][1000 genomes]
rs3770695	0.86[EUR][1000 genomes]
rs3770699	0.80[AMR][1000 genomes];0.95[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs3821136	0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3845633	0.85[EUR][1000 genomes]
rs3851937	0.85[AMR][1000 genomes];0.92[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs3856339	0.86[EUR][1000 genomes]
rs3863852	0.86[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4102441	0.86[AMR][1000 genomes];0.92[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs41272663	0.99[ASN][1000 genomes]
rs4467201	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4609985	0.89[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs4673526	0.96[EUR][1000 genomes]
rs4673528	0.80[EUR][1000 genomes]
rs4673529	0.83[EUR][1000 genomes]
rs6435568	0.88[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6435569	0.89[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6717228	0.86[AMR][1000 genomes];0.93[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs6745925	0.86[AMR][1000 genomes];0.92[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs6756422	0.86[EUR][1000 genomes]
rs725379	0.86[EUR][1000 genomes]
rs7575005	0.99[ASN][1000 genomes]
rs7578688	0.85[EUR][1000 genomes]
rs7595022	0.86[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1012567	chr2:211087588-211315554	Enhancers Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	6 gene(s)	inside rSNPs	diseases
2	nsv875767	chr2:211119233-211334647	Weak transcription Enhancers Genic enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	5 gene(s)	inside rSNPs	diseases
3	nsv3147	chr2:211281479-211326844	Weak transcription Enhancers Genic enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region lncRNA miRNA target site	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:211282200-211286800	Weak transcription	Psoas Muscle	Psoas
2	chr2:211282200-211286800	Weak transcription	Skeletal Muscle Female	skeletal muscle
3	chr2:211284200-211286200	Weak transcription	Fetal Heart	heart

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