Variant report

rSNPs within LD-proxies of this variant (count:20)

rs_ID	r²[population]
rs10138951	1.00[CEU][hapmap];0.83[EUR][1000 genomes]
rs11620910	1.00[CEU][hapmap];0.80[YRI][hapmap];0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs11623496	0.81[EUR][1000 genomes]
rs12323598	0.94[EUR][1000 genomes]
rs17110868	0.89[CEU][hapmap];0.96[EUR][1000 genomes]
rs55910446	0.87[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs57289554	0.96[EUR][1000 genomes]
rs57315708	0.92[EUR][1000 genomes]
rs57759210	0.94[EUR][1000 genomes]
rs61391568	0.94[EUR][1000 genomes]
rs6574591	0.89[CEU][hapmap];1.00[EUR][1000 genomes]
rs7156847	1.00[CEU][hapmap];0.80[YRI][hapmap];0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7157244	1.00[CEU][hapmap];0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7159335	1.00[CEU][hapmap];0.80[YRI][hapmap];0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73328690	0.93[EUR][1000 genomes]
rs8008286	1.00[CEU][hapmap];0.83[EUR][1000 genomes]
rs8008763	1.00[CEU][hapmap];0.98[EUR][1000 genomes]
rs8014976	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs8016841	0.88[CEU][hapmap];0.96[EUR][1000 genomes]
rs8017020	0.89[CEU][hapmap];0.96[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv869348	chr14:80921098-81535754	Weak transcription Strong transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
2	nsv565290	chr14:81085129-81230117	Weak transcription Enhancers Active TSS Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 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	chr14:81083400-81109400	Weak transcription	Dnd41	blood
2	chr14:81086600-81088600	Enhancers	Hela-S3	cervix
3	chr14:81087000-81088600	Enhancers	NHDF-Ad	bronchial
4	chr14:81087400-81104200	Weak transcription	HSMM	muscle
5	chr14:81087800-81088800	Enhancers	HUVEC	blood vessel
6	chr14:81088000-81088600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr14:81088200-81088600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
8	chr14:81088200-81088600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
9	chr14:81088200-81088600	Enhancers	Muscle Satellite Cultured Cells	--
10	chr14:81088200-81088600	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
11	chr14:81088200-81088600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
12	chr14:81088200-81088600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
13	chr14:81088200-81088600	Enhancers	NH-A	brain
14	chr14:81088200-81088600	Enhancers	NHEK	skin
15	chr14:81088200-81088600	Enhancers	Osteobl	bone
16	chr14:81088400-81088600	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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