Variant report

Variant	rs814634
Chromosome Location	chr10:90418065-90418066
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 43 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:36)

rs_ID	r²[population]
rs10736360	0.95[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap]
rs10736361	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1359581	0.94[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap];1.00[ASN][1000 genomes]
rs1409136	0.95[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap];1.00[ASN][1000 genomes]
rs1555839	0.90[CEU][hapmap]
rs1555842	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1594602	1.00[CHB][hapmap]
rs1653842	1.00[YRI][hapmap]
rs1653843	1.00[YRI][hapmap]
rs1653845	1.00[YRI][hapmap]
rs1769683	1.00[YRI][hapmap]
rs1769692	1.00[YRI][hapmap]
rs1980813	0.95[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap];1.00[ASN][1000 genomes]
rs2057641	0.88[AFR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2182304	0.88[AFR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2576155	0.95[CEU][hapmap];1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs2576163	0.81[CEU][hapmap]
rs2576167	0.95[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap]
rs2901950	0.91[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap]
rs376036	1.00[YRI][hapmap]
rs390436	1.00[YRI][hapmap]
rs407433	1.00[YRI][hapmap]
rs434401	1.00[YRI][hapmap]
rs442545	1.00[YRI][hapmap]
rs447416	1.00[YRI][hapmap]
rs451949	1.00[YRI][hapmap]
rs454439	1.00[YRI][hapmap]
rs701824	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs750508	0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7900987	0.88[AFR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7913742	1.00[ASN][1000 genomes]
rs7917696	1.00[ASN][1000 genomes]
rs814633	0.88[AFR][1000 genomes];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs814635	0.88[AFR][1000 genomes];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs860949	0.88[AFR][1000 genomes];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs875050	0.95[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv948664	chr10:90076715-90517150	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Bivalent Enhancer Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
2	nsv529324	chr10:90198865-90738588	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Active TSS Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	40 gene(s)	inside rSNPs	diseases
3	nsv430254	chr10:90265420-90500520	Flanking Active TSS Enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
4	nsv1044680	chr10:90316066-90466092	Enhancers Flanking Active TSS Weak transcription Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
5	nsv540740	chr10:90316066-90466092	Active TSS Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
6	nsv551839	chr10:90334835-90422136	Active TSS Flanking Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
7	nsv831941	chr10:90410488-90587332	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:17 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:90412800-90419400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
2	chr10:90415600-90423200	Weak transcription	Gastric	stomach
3	chr10:90417000-90418200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr10:90417000-90418200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
5	chr10:90417200-90418200	Enhancers	HMEC	breast
6	chr10:90417200-90418200	Enhancers	NHEK	skin
7	chr10:90417200-90418600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
8	chr10:90417200-90418600	Enhancers	NHDF-Ad	bronchial
9	chr10:90417400-90418600	Enhancers	Osteobl	bone
10	chr10:90417600-90418200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
11	chr10:90417600-90418200	Enhancers	NH-A	brain
12	chr10:90417600-90418600	Enhancers	Muscle Satellite Cultured Cells	--
13	chr10:90417600-90421800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
14	chr10:90417800-90418600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
15	chr10:90417800-90419600	Weak transcription	HSMM	muscle
16	chr10:90418000-90419600	Weak transcription	NHLF	lung
17	chr10:90418000-90420800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin

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