Variant report

rSNPs within LD-proxies of this variant (count:23)

rs_ID	r²[population]
rs10237149	0.89[ASN][1000 genomes]
rs10237280	0.89[ASN][1000 genomes]
rs10237366	0.89[ASN][1000 genomes]
rs10486314	0.90[ASN][1000 genomes]
rs11761877	0.83[AMR][1000 genomes];0.84[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12530943	0.83[AMR][1000 genomes]
rs12536081	0.81[AMR][1000 genomes];0.81[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12699994	0.87[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs12699999	0.99[ASN][1000 genomes]
rs13233322	0.89[ASN][1000 genomes]
rs13242358	0.81[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs13242758	0.81[AMR][1000 genomes]
rs2028015	0.82[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2286213	0.82[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs55761404	0.80[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs60976379	0.82[ASN][1000 genomes]
rs6461387	0.92[ASN][1000 genomes]
rs6461389	0.83[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs6461393	0.82[AMR][1000 genomes]
rs67248060	0.89[ASN][1000 genomes]
rs6973029	0.83[AMR][1000 genomes]
rs7794241	0.84[AMR][1000 genomes];0.81[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7801037	0.90[ASN][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	nsv498112	chr7:18677922-18991946	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription Genic enhancers ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	nsv887813	chr7:18720135-18995552	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	nsv523497	chr7:18896011-18959381	Weak transcription Flanking Active TSS Genic enhancers Enhancers ZNF genes & repeats Active TSS	TF binding region CpG island lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:18901600-18905600	Weak transcription	Muscle Satellite Cultured Cells	--
2	chr7:18901600-18905800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
3	chr7:18901800-18905200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
4	chr7:18901800-18905200	Weak transcription	NHDF-Ad	bronchial
5	chr7:18901800-18905600	Weak transcription	Osteobl	bone
6	chr7:18902000-18904800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
7	chr7:18903000-18940000	Weak transcription	Aorta	Aorta
8	chr7:18903800-18907400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
9	chr7:18904200-18904400	Enhancers	Adipose Nuclei	Adipose

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