Variant report

Variant	rs6943832
Chromosome Location	chr7:47914774-47914775
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 83 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:78)

rs_ID	r²[population]
rs10951932	0.81[AMR][1000 genomes]
rs10951935	0.89[AMR][1000 genomes]
rs11520726	0.89[AMR][1000 genomes]
rs12111689	0.83[AMR][1000 genomes]
rs12534916	0.89[AMR][1000 genomes]
rs12536468	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs17131867	0.81[AMR][1000 genomes]
rs17131869	0.81[AMR][1000 genomes]
rs17131893	0.86[AMR][1000 genomes]
rs17131896	0.86[AMR][1000 genomes]
rs17131899	0.86[AMR][1000 genomes]
rs17710983	0.85[CHB][hapmap];0.86[JPT][hapmap];0.81[ASN][1000 genomes]
rs2004959	0.89[AMR][1000 genomes]
rs2017282	0.89[AMR][1000 genomes]
rs2167876	0.80[AMR][1000 genomes]
rs2167877	0.89[AMR][1000 genomes]
rs2348656	0.89[AMR][1000 genomes]
rs2348657	0.89[AMR][1000 genomes]
rs2348658	0.89[AMR][1000 genomes]
rs2348659	0.89[AMR][1000 genomes]
rs2348660	0.89[AMR][1000 genomes]
rs2348661	0.89[AMR][1000 genomes]
rs2348662	0.89[AMR][1000 genomes]
rs2881990	0.89[AMR][1000 genomes]
rs35717990	0.86[AMR][1000 genomes]
rs3736548	0.89[AMR][1000 genomes]
rs3736549	0.89[AMR][1000 genomes]
rs4720619	0.89[AMR][1000 genomes]
rs4720620	0.89[AMR][1000 genomes]
rs4720621	0.89[AMR][1000 genomes]
rs4720622	0.89[AMR][1000 genomes]
rs4724653	0.89[AMR][1000 genomes]
rs4724654	0.89[AMR][1000 genomes]
rs4724655	0.89[AMR][1000 genomes]
rs4724656	0.89[AMR][1000 genomes]
rs4724657	0.89[AMR][1000 genomes]
rs4724658	0.89[AMR][1000 genomes]
rs4724660	0.89[AMR][1000 genomes]
rs4724661	0.89[AMR][1000 genomes]
rs5018488	0.80[AMR][1000 genomes]
rs59399629	0.89[AMR][1000 genomes]
rs62447060	0.81[AMR][1000 genomes]
rs62447061	0.81[AMR][1000 genomes]
rs62447062	0.89[AMR][1000 genomes]
rs62447070	0.89[AMR][1000 genomes]
rs62447081	0.81[AMR][1000 genomes]
rs62450661	0.81[ASN][1000 genomes]
rs62450662	0.81[AMR][1000 genomes]
rs62450663	0.81[AMR][1000 genomes]
rs62450665	0.81[AMR][1000 genomes]
rs62450666	0.81[AMR][1000 genomes]
rs62450667	0.81[AMR][1000 genomes]
rs62450668	0.81[AMR][1000 genomes]
rs6949590	0.80[AMR][1000 genomes]
rs6949762	0.97[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6950006	0.81[AMR][1000 genomes]
rs6950308	0.89[AMR][1000 genomes]
rs6955234	0.81[AMR][1000 genomes]
rs6958737	0.89[AMR][1000 genomes]
rs6959110	0.80[AMR][1000 genomes]
rs6961473	0.89[AMR][1000 genomes]
rs6965759	0.89[AMR][1000 genomes]
rs6970386	0.81[AMR][1000 genomes]
rs6970527	0.81[AMR][1000 genomes]
rs6972918	0.81[AMR][1000 genomes]
rs6977363	0.81[AMR][1000 genomes]
rs6977544	0.81[AMR][1000 genomes]
rs6977548	0.80[AMR][1000 genomes]
rs73105163	0.89[AMR][1000 genomes]
rs753432	0.89[AMR][1000 genomes]
rs7790593	0.87[AMR][1000 genomes];0.91[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs9690002	1.00[CEU][hapmap];0.93[CHB][hapmap];1.00[JPT][hapmap];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs9691249	0.86[AMR][1000 genomes]
rs9691411	1.00[CEU][hapmap];0.92[CHB][hapmap];1.00[JPT][hapmap];0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs9691425	0.90[AFR][1000 genomes];0.89[AMR][1000 genomes];0.96[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs9691969	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs9918570	0.89[AMR][1000 genomes]
rs9918571	0.89[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1026223	chr7:47560728-48243287	Genic enhancers Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
2	nsv869585	chr7:47765428-48151324	Flanking Active TSS Enhancers Strong transcription Bivalent/Poised TSS Weak transcription Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
3	nsv830991	chr7:47854530-48025996	Weak transcription Active TSS Genic enhancers Strong transcription Enhancers Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
4	nsv532120	chr7:47882757-48195869	Active TSS Flanking Active TSS Enhancers Strong transcription Weak transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
5	nsv606892	chr7:47903141-47930180	Enhancers Genic enhancers Weak transcription Strong transcription Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:47886800-47916000	Weak transcription	Right Ventricle	heart
2	chr7:47897200-47916000	Weak transcription	Left Ventricle	heart
3	chr7:47901200-47918200	Weak transcription	Right Atrium	heart
4	chr7:47902600-47916000	Weak transcription	Lung	lung
5	chr7:47903200-47922400	Weak transcription	Adipose Nuclei	Adipose
6	chr7:47903200-47923800	Weak transcription	Skeletal Muscle Male	skeletal muscle
7	chr7:47903400-47945000	Weak transcription	Brain Angular Gyrus	brain
8	chr7:47906200-47923000	Weak transcription	Skeletal Muscle Female	skeletal muscle
9	chr7:47913600-47929600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links