Variant report

Variant	rs6114638
Chromosome Location	chr20:24290502-24290503
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 81 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs57557589	0.86[EUR][1000 genomes]
rs59723501	1.00[EUR][1000 genomes]
rs6049565	0.88[EUR][1000 genomes]
rs60640318	1.00[EUR][1000 genomes]
rs6106819	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6106820	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6106821	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6106822	0.83[EUR][1000 genomes]
rs6106823	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6106824	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6106825	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6106833	1.00[EUR][1000 genomes]
rs6106834	1.00[EUR][1000 genomes]
rs6106835	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6106836	1.00[EUR][1000 genomes]
rs6106837	1.00[EUR][1000 genomes]
rs6106838	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6106839	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6106840	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6106841	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6106842	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6106843	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6106844	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6106845	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6106846	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6106847	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6106848	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6106849	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6106850	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6114592	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6114593	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6114594	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6114595	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6114596	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6114597	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6114598	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6114599	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6114601	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6114602	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6114604	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6114606	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6114612	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6114613	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6114616	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6114617	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6114618	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6114619	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6114627	1.00[EUR][1000 genomes]
rs6114629	1.00[EUR][1000 genomes]
rs6114630	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6114631	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6114632	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6114633	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6114634	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6114635	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6114636	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6114637	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6114639	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6114640	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6114641	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6114642	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6114643	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6114645	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6114646	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6114647	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6114648	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6114649	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6114650	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6114651	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6114652	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs61212262	1.00[EUR][1000 genomes]
rs73330483	1.00[EUR][1000 genomes]
rs73330497	1.00[EUR][1000 genomes]
rs73902774	1.00[EUR][1000 genomes]
rs73902777	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73902801	1.00[EUR][1000 genomes]
rs926995	1.00[EUR][1000 genomes]
rs926996	1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv9793	chr20:23939613-24734850	Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
2	nsv833945	chr20:24163437-24349462	Enhancers Active TSS Weak transcription ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers	TF binding region Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
3	nsv1058146	chr20:24210196-24531087	Bivalent Enhancer Weak transcription Flanking Active TSS Bivalent/Poised TSS Enhancers Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:24286400-24297000	Weak transcription	Primary T cells from cord blood	blood
2	chr20:24290000-24290800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
3	chr20:24290000-24291200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
4	chr20:24290200-24290800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr20:24290200-24290800	Enhancers	HMEC	breast
6	chr20:24290200-24291000	Enhancers	NHEK	skin

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