Variant report

Variant	rs72668822
Chromosome Location	chr4:121062952-121062953
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 52 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:48)

rs_ID	r²[population]
rs1526330	0.86[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs6821789	0.93[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs6833927	0.93[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs72668812	0.93[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs72668814	1.00[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs72668820	1.00[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs72668821	1.00[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs72668824	1.00[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs72668829	1.00[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs72668830	1.00[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs72668831	0.98[EUR][1000 genomes]
rs72668832	0.98[EUR][1000 genomes]
rs72668835	1.00[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs72668836	1.00[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs72668838	1.00[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs72668839	1.00[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs72668840	1.00[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs72668859	1.00[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs72668868	1.00[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs72668872	0.93[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs72668874	0.86[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs72668875	0.93[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs72668898	0.93[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs72668899	0.93[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs72668902	0.93[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs72670409	0.93[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs72670410	0.93[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs72670412	0.93[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs72670414	0.93[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs72670415	0.93[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs72670416	0.93[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs72670420	0.93[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs72670421	0.93[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs72670425	0.93[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs72670426	0.86[EUR][1000 genomes]
rs72670427	0.93[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs72670428	0.93[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs72670430	0.86[EUR][1000 genomes]
rs72670431	0.93[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs72670444	0.93[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs72670447	0.93[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs72670460	0.86[AMR][1000 genomes]
rs72670461	0.86[AMR][1000 genomes]
rs72670464	0.86[AMR][1000 genomes]
rs72670466	0.86[AMR][1000 genomes]
rs72670477	0.86[AMR][1000 genomes]
rs7662162	0.82[EUR][1000 genomes]
rs7673609	0.98[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	nsv532739	chr4:120392824-121098103	Enhancers Flanking Active TSS Strong transcription Weak transcription Bivalent/Poised TSS Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	33 gene(s)	inside rSNPs	diseases
2	nsv1007641	chr4:120884220-121555889	Strong transcription Active TSS Enhancers Flanking Active TSS Genic enhancers Weak transcription Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	24 gene(s)	inside rSNPs	diseases
3	nsv537234	chr4:120884220-121555889	Enhancers Weak transcription Genic enhancers Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	24 gene(s)	inside rSNPs	diseases
4	esv1845528	chr4:121034480-121185834	Active TSS Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:121061000-121065800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin

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