Variant report

Variant	rs9846818
Chromosome Location	chr3:48375685-48375686
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 85 )
Associated
traits (count: 34 )

rSNPs within LD-proxies of this variant (count:83)

rs_ID	r²[population]
rs1045482	0.85[AFR][1000 genomes];0.95[AMR][1000 genomes];0.92[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs11130162	0.87[AFR][1000 genomes];0.89[AMR][1000 genomes];0.91[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs11130163	0.81[AFR][1000 genomes];0.94[AMR][1000 genomes];0.92[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs11130164	0.84[EUR][1000 genomes]
rs1134867	0.89[AFR][1000 genomes];0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11706221	0.84[EUR][1000 genomes]
rs11706277	0.83[EUR][1000 genomes]
rs11707997	0.84[EUR][1000 genomes]
rs11710257	0.84[EUR][1000 genomes]
rs11713476	0.96[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs11714176	0.83[EUR][1000 genomes]
rs11714944	0.83[EUR][1000 genomes]
rs11715776	0.83[EUR][1000 genomes]
rs11716371	0.83[EUR][1000 genomes]
rs11716848	0.84[EUR][1000 genomes]
rs11717716	0.84[EUR][1000 genomes]
rs11718350	0.82[EUR][1000 genomes]
rs13060020	0.84[EUR][1000 genomes]
rs13061269	0.84[EUR][1000 genomes]
rs13066044	0.84[EUR][1000 genomes]
rs13066758	0.81[EUR][1000 genomes]
rs13067450	0.81[EUR][1000 genomes]
rs13069029	0.83[EUR][1000 genomes]
rs13070210	0.80[EUR][1000 genomes]
rs13071960	0.84[EUR][1000 genomes]
rs13079728	0.81[EUR][1000 genomes]
rs13081169	0.83[EUR][1000 genomes]
rs13081633	0.83[EUR][1000 genomes]
rs13082158	0.84[EUR][1000 genomes]
rs13082859	0.81[EUR][1000 genomes]
rs13084616	0.81[EUR][1000 genomes]
rs13085251	0.81[EUR][1000 genomes]
rs13090538	0.84[EUR][1000 genomes]
rs13095983	0.83[EUR][1000 genomes]
rs2541	0.81[EUR][1000 genomes]
rs3197223	0.81[EUR][1000 genomes]
rs34076262	0.84[EUR][1000 genomes]
rs34523942	0.81[EUR][1000 genomes]
rs34589064	0.81[EUR][1000 genomes]
rs34630841	0.81[EUR][1000 genomes]
rs34749846	0.81[EUR][1000 genomes]
rs34946886	0.81[EUR][1000 genomes]
rs35190747	0.81[EUR][1000 genomes]
rs35297395	0.81[EUR][1000 genomes]
rs35297486	0.81[EUR][1000 genomes]
rs35411187	0.83[EUR][1000 genomes]
rs35778847	0.81[EUR][1000 genomes]
rs35802497	0.81[EUR][1000 genomes]
rs35944878	0.80[EUR][1000 genomes]
rs36075665	0.81[EUR][1000 genomes]
rs36121690	0.81[EUR][1000 genomes]
rs4130522	0.83[EUR][1000 genomes]
rs4130995	0.98[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4371540	0.83[EUR][1000 genomes]
rs4392440	0.81[EUR][1000 genomes]
rs4420898	0.83[EUR][1000 genomes]
rs4479622	0.81[EUR][1000 genomes]
rs4511915	0.81[EUR][1000 genomes]
rs4511916	0.82[EUR][1000 genomes]
rs4541431	0.84[EUR][1000 genomes]
rs4619808	0.84[EUR][1000 genomes]
rs4632568	0.84[EUR][1000 genomes]
rs6442110	0.82[AFR][1000 genomes];0.93[AMR][1000 genomes];0.92[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs6782166	0.83[EUR][1000 genomes]
rs6787500	0.81[AFR][1000 genomes];0.88[AMR][1000 genomes];0.91[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs6793150	0.83[EUR][1000 genomes]
rs6793223	0.84[EUR][1000 genomes]
rs6793239	0.83[EUR][1000 genomes]
rs6804986	0.84[EUR][1000 genomes]
rs6806112	0.84[AFR][1000 genomes];0.85[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs71323394	0.83[EUR][1000 genomes]
rs71323395	0.84[EUR][1000 genomes]
rs71323396	0.84[EUR][1000 genomes]
rs71323397	0.84[EUR][1000 genomes]
rs7619865	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7621785	0.81[EUR][1000 genomes]
rs7624450	0.82[EUR][1000 genomes]
rs7632297	0.83[EUR][1000 genomes]
rs7645425	0.84[EUR][1000 genomes]
rs7652233	0.84[EUR][1000 genomes]
rs7653152	0.85[EUR][1000 genomes]
rs7653336	0.84[EUR][1000 genomes]
rs9825637	0.84[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	nsv834683	chr3:48301504-48493261	Weak transcription Active TSS Flanking Active TSS Strong transcription Enhancers ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	73 gene(s)	inside rSNPs	diseases
2	nsv967015	chr3:48370774-48381957	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

mRNA abundance (count:34)

SNP	Gene	Cis/trans	Tissue	Source
rs9846818	ZNF589	cis	Artery Aorta	GTEx
rs9846818	MAP4	Cis_1M	lymphoblastoid	RTeQTL
rs9846818	ZNF589	cis	Esophagus Mucosa	GTEx
rs9846818	NME6	cis	Nerve Tibial	GTEx
rs9846818	NME6	cis	Esophagus Muscularis	GTEx
rs9846818	MRPS18AP1	cis	Thyroid	GTEx
rs9846818	MRPS18AP1	cis	Artery Aorta	GTEx
rs9846818	MRPS18AP1	cis	Esophagus Mucosa	GTEx
rs9846818	CDC25A	cis	Adipose Subcutaneous	GTEx
rs9846818	MRPS18AP1	cis	Adipose Subcutaneous	GTEx
rs9846818	MRPS18AP1	cis	Esophagus Muscularis	GTEx
rs9846818	MRPS18AP1	cis	Artery Tibial	GTEx
rs9846818	ZNF589	cis	Artery Tibial	GTEx
rs9846818	CDC25A	cis	Muscle Skeletal	GTEx
rs9846818	MRPS18AP1	cis	Heart Left Ventricle	GTEx
rs9846818	ZNF589	cis	Skin Sun Exposed Lower leg	GTEx
rs9846818	ZNF589	cis	Thyroid	GTEx
rs9846818	MRPS18AP1	cis	Skin Sun Exposed Lower leg	GTEx
rs9846818	ZNF589	Cis_1M	lymphoblastoid	RTeQTL
rs9846818	MRPS18AP1	cis	Stomach	GTEx
rs9846818	MRPS18AP1	cis	Muscle Skeletal	GTEx
rs9846818	ZNF589	cis	Nerve Tibial	GTEx
rs9846818	ZNF589	cis	Whole Blood	GTEx
rs9846818	CDC25A	cis	Thyroid	GTEx
rs9846818	ZNF589	cis	lung	GTEx
rs9846818	MRPS18AP1	cis	Nerve Tibial	GTEx
rs9846818	CDC25A	cis	Artery Tibial	GTEx
rs9846818	MRPS18AP1	cis	lung	GTEx
rs9846818	NME6	cis	multi-tissue	Pritchard
rs9846818	ZNF589	cis	Stomach	GTEx
rs9846818	ZNF589	cis	Adipose Subcutaneous	GTEx
rs9846818	NME6	cis	Artery Aorta	GTEx
rs9846818	MRPS18AP1	cis	Whole Blood	GTEx
rs9846818	NME6	Cis_1M	lymphoblastoid	RTeQTL

Chromatin state (count:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:48372200-48377600	Enhancers	Placenta	Placenta
2	chr3:48374000-48376200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
3	chr3:48374000-48377400	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
4	chr3:48374400-48375800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
5	chr3:48374400-48375800	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
6	chr3:48374400-48377600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
7	chr3:48375000-48376600	Enhancers	Primary monocytes fromperipheralblood	blood
8	chr3:48375400-48377800	Enhancers	Primary B cells from cord blood	blood
9	chr3:48375600-48376400	Weak transcription	Primary hematopoietic stem cells	blood

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