Variant report

Variant	rs10745964
Chromosome Location	chr12:103788427-103788428
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 47 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:43)

rs_ID	r²[population]
rs10161272	0.91[AFR][1000 genomes];0.96[AMR][1000 genomes];0.94[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10745962	0.84[ASN][1000 genomes]
rs10745963	0.81[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs10745965	0.86[AFR][1000 genomes];0.96[AMR][1000 genomes];0.93[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10778240	0.81[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs10778241	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10778244	0.93[AMR][1000 genomes];0.92[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10778246	0.92[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs10860997	0.96[AMR][1000 genomes];0.91[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs10861000	0.96[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs10861005	0.92[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs10861013	0.86[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs10861015	0.86[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs10861016	0.86[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs11111551	0.87[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs11111555	0.97[AMR][1000 genomes];0.92[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11111556	0.96[AMR][1000 genomes];0.92[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs11111572	0.82[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs11111579	0.84[AMR][1000 genomes]
rs1320345	0.85[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs2374045	0.99[AFR][1000 genomes];0.97[AMR][1000 genomes];0.94[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2374056	0.92[AMR][1000 genomes];0.91[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs2374057	0.92[AMR][1000 genomes];0.91[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs2374062	0.84[ASN][1000 genomes]
rs2374065	0.91[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs2374078	0.82[AMR][1000 genomes]
rs2888733	0.85[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs6539073	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs7295887	0.91[AFR][1000 genomes];0.96[AMR][1000 genomes];0.94[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7298211	0.84[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs7300757	0.92[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs7301460	0.92[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs7302890	0.92[AMR][1000 genomes];0.92[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs7303147	0.92[AMR][1000 genomes];0.91[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs7304308	0.92[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs7312095	0.99[AFR][1000 genomes];0.97[AMR][1000 genomes];0.94[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7313836	0.86[AFR][1000 genomes];0.96[AMR][1000 genomes];0.93[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7313920	0.89[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs7952759	0.89[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs7967003	0.81[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs7967288	0.89[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs7970043	0.93[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs7970506	0.99[AFR][1000 genomes];0.97[AMR][1000 genomes];0.94[EUR][1000 genomes];0.99[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv455703	chr12:103692799-103818049	Flanking Active TSS Weak transcription Enhancers Active TSS Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Genic enhancers	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
2	nsv560037	chr12:103692799-103818049	Enhancers Bivalent Enhancer Strong transcription Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
3	nsv899477	chr12:103747515-103817326	Enhancers Strong transcription Weak transcription ZNF genes & repeats Active TSS Genic enhancers Bivalent Enhancer	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
4	nsv899478	chr12:103747515-103834275	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Genic enhancers	Chromatin interactive region lncRNA	1 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	chr12:103787000-103790400	Weak transcription	Primary B cells from cord blood	blood
2	chr12:103787200-103789800	Weak transcription	Primary B cells from peripheral blood	blood

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