Variant report

Variant	rs872167
Chromosome Location	chr12:42159641-42159642
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 43 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:35)

rs_ID	r²[population]
rs10748313	0.81[AMR][1000 genomes]
rs10785299	0.91[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs10880151	1.00[CEU][hapmap];0.94[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs10880154	1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10880166	0.90[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs10880169	0.89[AMR][1000 genomes]
rs11514058	0.87[AMR][1000 genomes]
rs12423162	0.89[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs12425223	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs12581243	0.90[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs12811639	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs1497162	0.90[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs1497173	0.90[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs1497187	0.85[AMR][1000 genomes];0.94[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1497189	0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1542828	0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1546192	0.91[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs1603537	0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs17129517	0.81[YRI][hapmap]
rs2173163	0.90[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs4569059	0.91[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs4595606	0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs4768008	0.97[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs4768009	0.93[AMR][1000 genomes];0.94[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs6582362	0.80[AMR][1000 genomes]
rs7138101	0.91[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7138161	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs7955116	0.90[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs7955211	0.90[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs7960024	0.89[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs7973978	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs7974787	0.89[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs872168	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs904076	0.91[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs904077	0.90[AMR][1000 genomes];0.94[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv899040	chr12:41905897-42181706	Enhancers Flanking Active TSS Weak transcription Active TSS Strong transcription Bivalent Enhancer ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
2	nsv832386	chr12:42017259-42189476	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	nsv899043	chr12:42058138-42313665	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
4	nsv899044	chr12:42058138-42321161	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
5	nsv899045	chr12:42118062-42174431	Weak transcription Enhancers ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
6	nsv975412	chr12:42158676-42161689	Enhancers Weak transcription	lncRNA	n/a	inside rSNPs	diseases
7	nsv1047870	chr12:42158954-42254373	Flanking Active TSS Weak transcription ZNF genes & repeats Enhancers Bivalent Enhancer	lncRNA	n/a	inside rSNPs	diseases
8	nsv1041975	chr12:42159517-42254373	Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription ZNF genes & repeats	lncRNA	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:42158600-42165600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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