Variant report

Variant	rs11041986
Chromosome Location	chr11:8582878-8582879
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr11:8581571..8583395-chr11:8585433..8587606,2	K562	blood:

Variant related genes	Relation type
ENSG00000130413	Chromatin interaction

Extended variants
information (count: 105 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:103)

rs_ID	r²[population]
rs10160430	0.99[ASN][1000 genomes]
rs10160804	0.86[AMR][1000 genomes];0.93[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs10160805	0.97[ASN][1000 genomes]
rs10743072	0.84[ASN][1000 genomes]
rs10743074	0.88[ASN][1000 genomes]
rs10743078	0.83[AMR][1000 genomes];0.92[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs10743079	0.83[AMR][1000 genomes];0.92[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs10743080	0.87[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs10743082	0.81[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs10769907	0.83[ASN][1000 genomes]
rs10769908	0.85[ASN][1000 genomes]
rs10769910	0.85[ASN][1000 genomes]
rs10769915	0.99[ASN][1000 genomes]
rs10769916	0.99[ASN][1000 genomes]
rs10769919	0.82[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs10769920	0.82[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs10769923	0.88[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs10769924	0.87[ASN][1000 genomes]
rs10769929	0.83[AMR][1000 genomes];0.81[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs10840047	0.83[ASN][1000 genomes]
rs10840051	0.84[ASN][1000 genomes]
rs10840055	0.84[ASN][1000 genomes]
rs10840056	0.84[ASN][1000 genomes]
rs10840058	0.85[ASN][1000 genomes]
rs10840060	0.85[ASN][1000 genomes]
rs10840065	0.88[ASN][1000 genomes]
rs10840072	0.90[ASN][1000 genomes]
rs10840077	0.97[ASN][1000 genomes]
rs10840079	0.85[EUR][1000 genomes]
rs10840080	0.88[ASN][1000 genomes]
rs10840081	0.82[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs10840084	0.95[ASN][1000 genomes]
rs10840087	0.89[ASN][1000 genomes]
rs10840089	0.87[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs11041924	0.81[ASN][1000 genomes]
rs11041929	0.83[EUR][1000 genomes]
rs11041962	0.90[ASN][1000 genomes]
rs11041974	0.94[ASN][1000 genomes]
rs11041983	0.81[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs11041985	0.81[AFR][1000 genomes];0.82[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs11041990	0.81[ASN][1000 genomes]
rs11041994	0.81[ASN][1000 genomes]
rs11041995	0.81[ASN][1000 genomes]
rs11041999	0.96[ASN][1000 genomes]
rs11042002	0.89[ASN][1000 genomes]
rs11493772	0.88[ASN][1000 genomes]
rs12226478	0.87[EUR][1000 genomes]
rs12576736	0.86[ASN][1000 genomes]
rs12785939	0.81[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs12805671	0.86[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs1374262	0.83[ASN][1000 genomes]
rs1374263	0.81[EUR][1000 genomes]
rs1446462	0.93[ASN][1000 genomes]
rs1446463	0.93[ASN][1000 genomes]
rs1446464	0.83[EUR][1000 genomes]
rs1900272	0.90[AMR][1000 genomes];0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1900273	0.84[ASN][1000 genomes]
rs2015629	0.93[ASN][1000 genomes]
rs2044463	0.83[ASN][1000 genomes]
rs2289921	0.84[ASN][1000 genomes]
rs2289923	0.83[EUR][1000 genomes]
rs2871753	0.85[ASN][1000 genomes]
rs3969875	0.80[ASN][1000 genomes]
rs4131072	0.81[AMR][1000 genomes];0.92[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs4244806	0.82[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs4405311	0.85[EUR][1000 genomes]
rs4418812	0.96[ASN][1000 genomes]
rs4520598	0.86[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs4758067	0.83[EUR][1000 genomes]
rs4929929	0.83[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs4929941	0.88[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs4929942	0.87[ASN][1000 genomes]
rs4929949	0.95[ASN][1000 genomes]
rs4929950	0.82[AMR][1000 genomes];0.92[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs6578968	0.84[ASN][1000 genomes]
rs6578969	0.84[ASN][1000 genomes]
rs7101471	0.83[ASN][1000 genomes]
rs7112153	0.84[ASN][1000 genomes]
rs7120065	0.85[ASN][1000 genomes]
rs7126013	0.83[EUR][1000 genomes]
rs7127684	0.83[ASN][1000 genomes]
rs7129357	0.82[EUR][1000 genomes]
rs726007	0.82[EUR][1000 genomes]
rs7924753	0.85[ASN][1000 genomes]
rs7929120	0.81[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs7931604	0.83[EUR][1000 genomes]
rs7934396	0.89[ASN][1000 genomes]
rs7935708	0.83[ASN][1000 genomes]
rs7947670	0.88[ASN][1000 genomes]
rs7949017	0.83[ASN][1000 genomes]
rs7950870	0.90[ASN][1000 genomes]
rs9284150	0.81[AMR][1000 genomes];0.90[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs9284151	0.82[AMR][1000 genomes];0.92[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs9300088	0.86[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs9300089	0.95[AMR][1000 genomes];0.95[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs9300090	0.99[ASN][1000 genomes]
rs9300091	0.81[AFR][1000 genomes];0.82[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs9300094	0.82[AMR][1000 genomes];0.92[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs9705083	0.81[ASN][1000 genomes]
rs9705253	0.96[ASN][1000 genomes]
rs9736791	0.98[AFR][1000 genomes];0.86[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs9737312	0.82[ASN][1000 genomes]
rs9737401	0.90[ASN][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	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:1)

SNP	Gene	Cis/trans	Tissue	Source
rs11041986	STK33	cis	Artery Tibial	GTEx

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:8580400-8588600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr11:8582600-8584000	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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