Variant report

rSNPs within LD-proxies of this variant (count:31)

rs_ID	r²[population]
rs11751885	0.83[EUR][1000 genomes]
rs11753657	0.83[EUR][1000 genomes]
rs11755342	0.83[EUR][1000 genomes]
rs11756326	0.84[EUR][1000 genomes]
rs11759337	0.82[EUR][1000 genomes]
rs16890184	0.83[EUR][1000 genomes]
rs17332393	0.82[EUR][1000 genomes]
rs55644721	0.81[EUR][1000 genomes]
rs55858016	0.82[EUR][1000 genomes]
rs55883909	0.87[EUR][1000 genomes]
rs62426506	1.00[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs62426508	0.82[EUR][1000 genomes]
rs62426527	1.00[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs62426531	1.00[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs62426535	0.88[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs62426551	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs62426552	0.84[EUR][1000 genomes]
rs62426553	0.86[EUR][1000 genomes]
rs62426554	0.80[EUR][1000 genomes]
rs9294120	0.83[EUR][1000 genomes]
rs9443600	0.87[EUR][1000 genomes]
rs9443601	0.83[EUR][1000 genomes]
rs9443602	0.83[EUR][1000 genomes]
rs9448490	0.82[EUR][1000 genomes]
rs9448492	0.83[EUR][1000 genomes]
rs9448495	0.83[EUR][1000 genomes]
rs9448498	0.83[EUR][1000 genomes]
rs9448499	0.83[EUR][1000 genomes]
rs9448500	0.83[EUR][1000 genomes]
rs9448505	0.80[EUR][1000 genomes]
rs9448508	0.83[EUR][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	nsv886235	chr6:78861808-79369972	Enhancers Active TSS Weak transcription ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
2	nsv604011	chr6:79042990-79455282	Enhancers Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
3	nsv886300	chr6:79129963-79341891	Enhancers Active TSS Weak transcription Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
4	nsv522646	chr6:79185106-79333988	Enhancers Flanking Active TSS Weak transcription Active TSS Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
5	nsv1028767	chr6:79200713-79341224	Enhancers Active TSS Weak transcription Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:16 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:79307400-79308200	Weak transcription	HSMM	muscle
2	chr6:79307400-79309800	Enhancers	NH-A	brain
3	chr6:79307400-79310000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
4	chr6:79307400-79310000	Enhancers	HMEC	breast
5	chr6:79307400-79310000	Enhancers	NHLF	lung
6	chr6:79307400-79310600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
7	chr6:79307400-79310800	Enhancers	NHEK	skin
8	chr6:79307600-79308400	Enhancers	Placenta Amnion	Placenta Amnion
9	chr6:79307600-79310800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
10	chr6:79307600-79311200	Enhancers	HUVEC	blood vessel
11	chr6:79307800-79308400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
12	chr6:79307800-79308400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
13	chr6:79307800-79308800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
14	chr6:79307800-79309000	Enhancers	Ovary	ovary
15	chr6:79307800-79309800	Enhancers	A549	lung
16	chr6:79307800-79310000	Enhancers	Hela-S3	cervix

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