Variant report

Variant	rs4803509
Chromosome Location	chr19:38288724-38288725
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 56 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:51)

rs_ID	r²[population]
rs10048511	0.90[ASN][1000 genomes]
rs10401637	0.92[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs10401968	0.95[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs10402530	0.96[AFR][1000 genomes];0.93[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs10404567	0.81[EUR][1000 genomes]
rs10409402	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10409487	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10420746	0.90[ASN][1000 genomes]
rs10420891	0.89[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs10427125	0.92[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs11673023	0.86[ASN][1000 genomes]
rs11878269	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11879180	0.91[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs1291	0.84[ASN][1000 genomes]
rs12974225	0.88[ASN][1000 genomes]
rs12975057	0.91[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs171376	0.84[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs1974714	0.83[ASN][1000 genomes]
rs2075281	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2075283	0.84[ASN][1000 genomes]
rs241932	0.82[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs241933	0.80[ASN][1000 genomes]
rs241950	0.84[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2909100	0.81[ASN][1000 genomes]
rs2972437	0.83[ASN][1000 genomes]
rs2972438	0.83[ASN][1000 genomes]
rs2972439	0.83[ASN][1000 genomes]
rs2972445	0.83[ASN][1000 genomes]
rs3095726	0.84[ASN][1000 genomes]
rs35209753	0.83[EUR][1000 genomes]
rs3848625	0.82[ASN][1000 genomes]
rs3848626	0.97[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs4802135	0.89[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs4803524	0.86[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs58449039	0.95[AFR][1000 genomes];0.91[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs6508742	0.87[AMR][1000 genomes];0.87[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7250571	0.92[AFR][1000 genomes];0.92[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs7250868	0.89[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs7252010	0.86[AFR][1000 genomes];0.91[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs7257125	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs7258597	0.81[EUR][1000 genomes]
rs8101752	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs8101858	0.96[AFR][1000 genomes];0.91[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs8102579	0.96[AFR][1000 genomes];0.92[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs8103633	0.84[ASN][1000 genomes]
rs8104076	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs8112706	0.83[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs8182498	0.91[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs856300	0.81[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs856304	0.83[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs9304569	0.87[AMR][1000 genomes];0.87[EUR][1000 genomes];0.93[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 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
3	nsv833820	chr19:38190721-38414049	Flanking Active TSS Weak transcription ZNF genes & repeats Strong transcription Active TSS Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	27 gene(s)	inside rSNPs	diseases
4	nsv960835	chr19:38270238-38293706	Active TSS ZNF genes & repeats Weak transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
5	nsv1057428	chr19:38282158-38320814	Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Active TSS Weak transcription Flanking Active TSS Strong transcription Enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs4803509	WDR87	cis	Thyroid	GTEx

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:38285400-38288800	ZNF genes & repeats	Liver	Liver

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