Variant report

Variant	rs9374663
Chromosome Location	chr6:117782634-117782635
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 50 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:49)

rs_ID	r²[population]
rs10782186	0.83[CHB][hapmap];0.80[JPT][hapmap]
rs1321798	0.96[CEU][hapmap];0.85[EUR][1000 genomes]
rs1321799	0.96[CEU][hapmap];0.85[EUR][1000 genomes]
rs1321802	0.96[CEU][hapmap];0.84[EUR][1000 genomes]
rs1321803	0.82[EUR][1000 genomes]
rs1321815	0.90[EUR][1000 genomes]
rs1321816	0.89[EUR][1000 genomes]
rs1407179	0.84[CEU][hapmap]
rs1407184	0.90[JPT][hapmap]
rs1407185	0.85[EUR][1000 genomes]
rs1853148	0.85[AMR][1000 genomes];0.96[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2057314	0.83[CHB][hapmap];0.82[JPT][hapmap]
rs2180811	1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2243	0.90[JPT][hapmap]
rs2243378	0.96[CEU][hapmap];0.81[EUR][1000 genomes]
rs2273602	0.96[CEU][hapmap];0.85[EUR][1000 genomes]
rs34882116	0.87[AMR][1000 genomes];0.93[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs3777981	0.96[CEU][hapmap];0.81[CHB][hapmap];0.89[EUR][1000 genomes]
rs3798390	0.85[EUR][1000 genomes]
rs3798393	0.96[CEU][hapmap];0.85[EUR][1000 genomes]
rs3798394	0.96[CEU][hapmap];0.85[EUR][1000 genomes]
rs4945584	0.86[AMR][1000 genomes];0.96[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs4945586	0.83[CHB][hapmap];0.82[JPT][hapmap]
rs4946254	0.95[JPT][hapmap];0.88[ASN][1000 genomes]
rs4946256	0.91[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4946260	0.83[CHB][hapmap];0.80[JPT][hapmap]
rs6911915	0.83[CHB][hapmap]
rs6937083	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6941337	0.90[ASN][1000 genomes]
rs765516	0.96[CEU][hapmap];0.85[EUR][1000 genomes]
rs7770923	0.96[CEU][hapmap];0.85[EUR][1000 genomes]
rs7771211	0.96[CEU][hapmap];0.85[EUR][1000 genomes]
rs7771271	0.85[EUR][1000 genomes]
rs7771637	0.81[JPT][hapmap];0.85[EUR][1000 genomes]
rs7772046	0.96[CEU][hapmap];0.85[EUR][1000 genomes]
rs7776244	0.96[CEU][hapmap];0.85[EUR][1000 genomes]
rs929057	0.83[CHB][hapmap];0.81[JPT][hapmap]
rs9320604	0.83[CHB][hapmap];0.80[JPT][hapmap]
rs9372480	0.85[AMR][1000 genomes];0.96[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs9374658	0.90[JPT][hapmap]
rs9374662	1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9385012	0.85[EUR][1000 genomes]
rs9385013	0.84[EUR][1000 genomes]
rs9387478	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9401006	0.96[CEU][hapmap];0.85[EUR][1000 genomes]
rs9401007	0.85[EUR][1000 genomes]
rs9481728	0.83[CHB][hapmap];0.82[JPT][hapmap]
rs9489150	0.81[EUR][1000 genomes]
rs9489152	0.89[CEU][hapmap]

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	nsv532050	chr6:117528154-118203005	ZNF genes & repeats Enhancers Bivalent Enhancer Active TSS Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs9374663	DCBLD1	cis	Thyroid	GTEx

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:117781000-117785000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
2	chr6:117782400-117784600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin

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