Variant report

rSNPs within LD-proxies of this variant (count:30)

rs_ID	r²[population]
rs10093150	0.90[ASN][1000 genomes]
rs10435554	0.83[AMR][1000 genomes]
rs10956463	0.86[ASN][1000 genomes]
rs10956464	0.90[ASN][1000 genomes]
rs10956465	0.94[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12541644	0.88[AMR][1000 genomes]
rs12546355	0.84[ASN][1000 genomes]
rs13270479	0.88[ASN][1000 genomes]
rs4289775	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4333552	0.82[AMR][1000 genomes]
rs4448233	0.82[ASN][1000 genomes]
rs4524751	0.84[ASN][1000 genomes]
rs4524752	0.84[ASN][1000 genomes]
rs6470696	0.84[ASN][1000 genomes]
rs6470698	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6981888	0.86[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6982195	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6987260	0.84[ASN][1000 genomes]
rs6989490	0.83[AMR][1000 genomes]
rs6996505	0.90[ASN][1000 genomes]
rs6996806	0.85[AMR][1000 genomes]
rs7001827	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7007293	0.84[ASN][1000 genomes]
rs7011330	0.84[ASN][1000 genomes]
rs72609876	0.98[ASN][1000 genomes]
rs7815753	0.88[ASN][1000 genomes]
rs7821655	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7824972	0.84[ASN][1000 genomes]
rs7831436	0.88[ASN][1000 genomes]
rs7839556	0.83[AFR][1000 genomes];0.93[AMR][1000 genomes];0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv891443	chr8:130016499-130220746	Weak transcription Flanking Active TSS Enhancers Genic enhancers Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats Active TSS	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:130126400-130160600	Weak transcription	Fetal Thymus	thymus
2	chr8:130146000-130158800	Genic enhancers	Dnd41	blood
3	chr8:130148400-130149200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
4	chr8:130148400-130149400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
5	chr8:130148400-130149600	Weak transcription	Fetal Muscle Leg	muscle
6	chr8:130148600-130149600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
7	chr8:130148800-130149200	Enhancers	Muscle Satellite Cultured Cells	--
8	chr8:130149000-130149400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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