Variant report

Variant	rs7119274
Chromosome Location	chr11:8546365-8546366
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 31 )
Associated
traits (count: 7 )

rSNPs within LD-proxies of this variant (count:29)

rs_ID	r²[population]
rs10743075	0.80[ASN][1000 genomes]
rs11041927	0.81[CHB][hapmap];0.83[JPT][hapmap]
rs11041929	0.83[YRI][hapmap]
rs11041939	0.87[CHB][hapmap];0.84[JPT][hapmap]
rs11041943	0.87[CHB][hapmap];0.84[JPT][hapmap]
rs11041949	0.91[AFR][1000 genomes];0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs11041955	0.88[AMR][1000 genomes];0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs11041960	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11041966	0.87[CHB][hapmap];0.88[CHD][hapmap];0.84[JPT][hapmap]
rs11041982	1.00[YRI][hapmap]
rs11820339	0.85[CEU][hapmap]
rs12224971	0.81[CHB][hapmap];0.84[JPT][hapmap]
rs12226069	0.86[AFR][1000 genomes];0.95[ASN][1000 genomes]
rs12226478	0.84[AFR][1000 genomes]
rs12576961	0.91[AFR][1000 genomes];0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12806736	0.89[LWK][hapmap];0.88[MKK][hapmap];0.95[YRI][hapmap]
rs1446464	0.82[YRI][hapmap]
rs1992756	0.93[ASW][hapmap];1.00[CEU][hapmap];0.94[CHB][hapmap];0.92[CHD][hapmap];0.94[GIH][hapmap];0.89[JPT][hapmap];0.95[LWK][hapmap];1.00[MEX][hapmap];0.85[MKK][hapmap];1.00[TSI][hapmap]
rs2028881	1.00[CEU][hapmap];0.94[CHB][hapmap];0.94[JPT][hapmap];0.95[YRI][hapmap]
rs2311390	0.93[ASW][hapmap];1.00[CEU][hapmap];0.94[CHB][hapmap];0.92[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];0.93[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.94[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4586148	0.81[CHB][hapmap]
rs4758067	0.84[MKK][hapmap];0.82[YRI][hapmap]
rs4929950	0.82[YRI][hapmap]
rs7105027	1.00[ASW][hapmap];1.00[CEU][hapmap];0.94[CHB][hapmap];0.92[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.95[LWK][hapmap];1.00[MEX][hapmap];0.93[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.97[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs726007	0.87[ASW][hapmap]
rs73405938	0.93[AFR][1000 genomes];0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7931604	0.80[YRI][hapmap]
rs7950041	0.85[AMR][1000 genomes];0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9284150	0.82[YRI][hapmap]

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	esv2751035	chr11:8431654-8685451	Strong transcription Weak transcription Enhancers ZNF genes & repeats Genic enhancers Flanking Active TSS Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
2	nsv896983	chr11:8526643-8682465	ZNF genes & repeats Strong transcription Weak transcription Bivalent Enhancer Flanking Active TSS Enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases

mRNA abundance (count:7)

SNP	Gene	Cis/trans	Tissue	Source
rs7119274	STK33	cis	lymphoblastoid	seeQTL
rs7119274	RPL27A	cis	parietal	SCAN
rs7119274	OR52W1	cis	parietal	SCAN
rs7119274	RNF141	cis	cerebellum	SCAN
rs7119274	OR51L1	cis	cerebellum	SCAN
rs7119274	CSNK2A1P	cis	cerebellum	SCAN
rs7119274	LYVE1	cis	cerebellum	SCAN

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:8545400-8549600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr11:8546000-8549600	Weak transcription	Fetal Heart	heart

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