Variant report

Variant	rs4913512
Chromosome Location	chr12:67321354-67321355
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 49 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:40)

rs_ID	r²[population]
rs10506514	0.86[CEU][hapmap];0.81[EUR][1000 genomes]
rs10506515	0.81[CEU][hapmap];0.81[EUR][1000 genomes]
rs10878520	0.81[EUR][1000 genomes]
rs10878521	0.81[EUR][1000 genomes]
rs10878522	0.81[EUR][1000 genomes]
rs10878523	0.86[CEU][hapmap];0.81[EUR][1000 genomes]
rs10878524	0.90[CEU][hapmap]
rs10878525	0.81[EUR][1000 genomes]
rs10878526	0.81[EUR][1000 genomes]
rs10878527	0.81[EUR][1000 genomes]
rs10878528	0.81[EUR][1000 genomes]
rs10878529	0.81[EUR][1000 genomes]
rs10878530	0.81[EUR][1000 genomes]
rs10878531	0.81[EUR][1000 genomes]
rs10878532	0.81[EUR][1000 genomes]
rs10878533	0.81[EUR][1000 genomes]
rs10878534	0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs11176482	0.81[EUR][1000 genomes]
rs11176483	0.81[EUR][1000 genomes]
rs11176484	0.86[CEU][hapmap];0.81[EUR][1000 genomes]
rs11176487	0.88[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs12228305	0.86[CEU][hapmap]
rs12228327	0.81[EUR][1000 genomes]
rs12229513	0.81[EUR][1000 genomes]
rs12579822	0.81[EUR][1000 genomes]
rs12579830	0.81[EUR][1000 genomes]
rs12580443	0.81[EUR][1000 genomes]
rs12581024	0.86[EUR][1000 genomes]
rs12811743	0.85[EUR][1000 genomes]
rs12811914	0.85[EUR][1000 genomes]
rs1504313	0.94[AFR][1000 genomes];0.87[AMR][1000 genomes];0.94[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs1875832	0.83[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1995503	0.86[CEU][hapmap];0.81[EUR][1000 genomes]
rs1995504	0.86[CEU][hapmap];0.81[EUR][1000 genomes]
rs2221396	0.81[EUR][1000 genomes]
rs2870925	0.85[AMR][1000 genomes];0.96[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2904532	0.81[EUR][1000 genomes]
rs6581722	0.89[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs7299111	0.88[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs962415	0.82[CEU][hapmap];0.96[GIH][hapmap];0.86[MEX][hapmap];0.92[TSI][hapmap];0.88[AMR][1000 genomes];0.86[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1040682	chr12:66750103-67328053	Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Strong transcription Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
2	nsv1053250	chr12:67067995-67381411	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	nsv1037144	chr12:67203280-67325187	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
4	nsv1044939	chr12:67207260-67377982	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Strong transcription	Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
5	nsv1036984	chr12:67273098-67427543	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription	Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
6	nsv1054433	chr12:67302689-67357930	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
7	nsv541523	chr12:67302689-67357930	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
8	nsv521008	chr12:67305277-67322614	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
9	nsv541524	chr12:67311057-67700349	Strong transcription Enhancers Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs4913512	DYRK2	cis	parietal	SCAN

Chromatin state (count:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:67315600-67327800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr12:67317800-67323000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr12:67319200-67322600	Weak transcription	Primary T helper cells PMA-I stimulated	--
4	chr12:67320200-67322000	Enhancers	Breast Myoepithelial Primary Cells	Breast
5	chr12:67320400-67328200	Weak transcription	Placenta	Placenta
6	chr12:67320800-67323800	Enhancers	Primary T cells from cord blood	blood
7	chr12:67321200-67321400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
8	chr12:67321200-67321600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr12:67321200-67322200	Enhancers	Brain Germinal Matrix	brain

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links