Variant report

Variant	rs2667477
Chromosome Location	chr12:84023388-84023389
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 61 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:58)

rs_ID	r²[population]
rs10779016	0.90[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs10862729	0.91[ASN][1000 genomes]
rs10862732	0.91[ASN][1000 genomes]
rs11115937	0.89[AFR][1000 genomes];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11115951	0.93[AMR][1000 genomes]
rs11115954	0.89[AMR][1000 genomes];0.90[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11115987	0.83[AMR][1000 genomes];0.83[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs11115988	0.91[ASN][1000 genomes]
rs11115992	0.91[ASN][1000 genomes]
rs11115993	0.91[ASN][1000 genomes]
rs11115996	0.91[ASN][1000 genomes]
rs11531162	0.91[ASN][1000 genomes]
rs11533593	0.91[ASN][1000 genomes]
rs11561341	0.91[ASN][1000 genomes]
rs1156937	0.87[AMR][1000 genomes]
rs1156938	0.90[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs11832354	0.91[ASN][1000 genomes]
rs11833515	0.91[ASN][1000 genomes]
rs12231539	0.89[AMR][1000 genomes]
rs12301047	0.91[ASN][1000 genomes]
rs1397893	0.90[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1397894	0.90[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1497341	0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1497348	0.94[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1497349	0.93[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1511581	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1511585	0.90[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs1603574	0.91[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1841343	0.91[ASN][1000 genomes]
rs1841344	0.91[ASN][1000 genomes]
rs1841345	0.91[ASN][1000 genomes]
rs1841346	0.91[ASN][1000 genomes]
rs1841347	0.91[ASN][1000 genomes]
rs1858328	0.91[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1903302	0.91[ASN][1000 genomes]
rs1903303	0.81[AMR][1000 genomes];0.82[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2169177	0.91[ASN][1000 genomes]
rs2173190	0.90[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs2645976	0.93[AMR][1000 genomes];0.93[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs324766	0.84[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs324771	0.98[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs365870	0.84[AFR][1000 genomes];0.87[AMR][1000 genomes];0.94[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs392087	0.81[AFR][1000 genomes];0.87[AMR][1000 genomes];0.94[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs398380	0.84[AFR][1000 genomes];0.87[AMR][1000 genomes];0.94[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs3993343	0.91[ASN][1000 genomes]
rs421713	0.95[AMR][1000 genomes];0.93[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4882398	0.91[ASN][1000 genomes]
rs56172305	0.91[ASN][1000 genomes]
rs58417914	0.81[AMR][1000 genomes];0.83[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs67932408	0.81[AMR][1000 genomes];0.83[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs68077020	0.91[ASN][1000 genomes]
rs7297591	0.91[ASN][1000 genomes]
rs7301076	0.91[ASN][1000 genomes]
rs7961422	0.88[AMR][1000 genomes];0.92[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs7962126	0.90[AMR][1000 genomes];0.91[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7964886	0.90[AMR][1000 genomes]
rs904091	0.90[EUR][1000 genomes]
rs990646	0.97[AMR][1000 genomes];0.93[EUR][1000 genomes];0.98[ASN][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	nsv469496	chr12:84014359-84074475	Active TSS Enhancers Weak transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
2	nsv559562	chr12:84014359-84074475	Enhancers Weak transcription ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
3	nsv559563	chr12:84017043-84450824	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Bivalent Enhancer Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:84022200-84024400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr12:84022200-84024800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived

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