Variant report

Variant	rs9367566
Chromosome Location	chr6:54226340-54226341
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 38 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:35)

rs_ID	r²[population]
rs10456682	0.86[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs10484642	0.82[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs10498797	0.84[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs10948812	0.84[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs10948813	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10948814	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12189890	0.86[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs12193891	0.84[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs12195997	0.82[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs12204930	0.86[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs12205456	0.84[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs12209457	0.84[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs12210322	0.86[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs12215711	0.84[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs12661397	0.84[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs12663327	0.84[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs12664425	0.86[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs16885285	0.82[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs2063238	0.86[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs3195579	0.84[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs3736350	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3777640	0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs45545344	0.84[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs59459598	0.86[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs59508393	0.86[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs62412590	0.82[EUR][1000 genomes]
rs62412614	0.84[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs62412618	0.82[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs73446621	0.84[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs7750024	0.86[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs7750323	0.80[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs9395943	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9395949	0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs9474819	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9474825	0.84[AMR][1000 genomes];0.95[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	nsv1067663	chr6:53796341-54449718	Enhancers Active TSS Weak transcription Strong transcription Flanking Active TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
2	nsv529158	chr6:53796341-54449718	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
3	nsv885888	chr6:54132353-54266032	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:54211800-54256200	Weak transcription	Fetal Intestine Large	intestine
2	chr6:54212000-54257400	Weak transcription	Rectal Mucosa Donor 31	rectum
3	chr6:54225800-54227200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
4	chr6:54226000-54226800	Enhancers	HMEC	breast
5	chr6:54226000-54227200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr6:54226000-54227200	Enhancers	NHEK	skin
7	chr6:54226200-54226600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin

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