Variant report

Variant	rs74063030
Chromosome Location	chr14:72512427-72512428
allele	A/G
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]
rs11844223	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11844287	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11845023	0.85[AFR][1000 genomes];0.81[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11846804	0.81[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs11846808	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11846932	1.00[EUR][1000 genomes]
rs11846989	1.00[EUR][1000 genomes]
rs11847719	1.00[EUR][1000 genomes]
rs11847881	1.00[EUR][1000 genomes]
rs11848888	1.00[EUR][1000 genomes]
rs11849072	1.00[EUR][1000 genomes]
rs11850119	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11850239	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11851082	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11851575	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11852228	1.00[EUR][1000 genomes]
rs17768491	0.96[EUR][1000 genomes]
rs2012352	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2012354	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4262883	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4374087	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4383069	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4899416	1.00[EUR][1000 genomes]
rs4899417	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4899418	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4902980	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs56098489	1.00[EUR][1000 genomes]
rs56879125	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs57851285	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs58117647	0.96[EUR][1000 genomes]
rs59008832	1.00[EUR][1000 genomes]
rs60103614	0.92[EUR][1000 genomes]
rs60517172	1.00[EUR][1000 genomes]
rs734424	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs734425	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs734426	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs734427	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs74060456	1.00[EUR][1000 genomes]
rs74060461	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs74060463	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs74060464	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs74063009	1.00[EUR][1000 genomes]
rs74063026	0.93[AFR][1000 genomes];0.81[AMR][1000 genomes];1.00[EUR][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	nsv530794	chr14:72113818-73034008	Enhancers Bivalent/Poised TSS Weak transcription Strong transcription Flanking Active TSS Genic enhancers Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	8 gene(s)	inside rSNPs	diseases
2	nsv948800	chr14:72462557-73150701	Enhancers Bivalent Enhancer Weak transcription Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	11 gene(s)	inside rSNPs	diseases
3	nsv1053520	chr14:72485195-72537202	Weak transcription Enhancers Flanking Active TSS Strong transcription Active TSS ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
4	esv3443786	chr14:72512284-72512644	Enhancers Strong transcription	n/a	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:72512200-72513400	Strong transcription	Cortex derived primary cultured neurospheres	brain
2	chr14:72512400-72512800	Enhancers	Left Ventricle	heart

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