Variant report

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

rs_ID	r²[population]
rs1060522	0.87[EUR][1000 genomes]
rs10853710	0.90[EUR][1000 genomes]
rs11083429	0.82[EUR][1000 genomes]
rs11083433	0.87[EUR][1000 genomes]
rs11666172	0.90[EUR][1000 genomes]
rs11668796	0.83[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11671953	0.98[EUR][1000 genomes]
rs11673497	1.00[EUR][1000 genomes]
rs16975299	0.87[EUR][1000 genomes]
rs17246792	0.98[EUR][1000 genomes]
rs28431170	1.00[EUR][1000 genomes]
rs2891657	0.87[EUR][1000 genomes]
rs34991303	0.91[EUR][1000 genomes]
rs55871826	0.99[EUR][1000 genomes]
rs55950325	0.87[EUR][1000 genomes]
rs62108305	0.98[EUR][1000 genomes]
rs62108351	0.87[EUR][1000 genomes]
rs6508739	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7249622	0.91[EUR][1000 genomes]
rs7253081	0.91[EUR][1000 genomes]
rs7258385	0.98[EUR][1000 genomes]
rs73037060	0.96[EUR][1000 genomes]
rs8102818	0.82[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	nsv579468	chr19:37977609-38293487	ZNF genes & repeats Strong transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Active TSS Weak transcription Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	28 gene(s)	inside rSNPs	diseases
2	nsv949296	chr19:38034722-38763140	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Strong transcription Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	58 gene(s)	inside rSNPs	diseases

mRNA abundance (count:2)

SNP	Gene	Cis/trans	Tissue	Source
rs55913702	AC012309.5	cis	Thyroid	GTEx
rs55913702	ZNF573	cis	multi-tissue	Pritchard

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:38152000-38169000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
2	chr19:38156600-38165200	ZNF genes & repeats	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
3	chr19:38156600-38165200	ZNF genes & repeats	Duodenum Smooth Muscle	Duodenum
4	chr19:38159200-38165200	ZNF genes & repeats	Adipose Nuclei	Adipose
5	chr19:38161000-38164400	Weak transcription	Ovary	ovary
6	chr19:38164000-38165000	ZNF genes & repeats	Left Ventricle	heart

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