Variant report

Variant	rs13064883
Chromosome Location	chr3:48952284-48952285
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr3:48945423..48948867-chr3:48951385..48953523,3	K562	blood:
2	chr3:48948534..48952570-chr3:48954278..48957832,4	MCF-7	breast:

Variant related genes	Relation type
ENSG00000177479	Chromatin interaction
ENSG00000221883	Chromatin interaction

Extended variants
information (count: 83 )
Associated
traits (count: 24 )

rSNPs within LD-proxies of this variant (count:80)

rs_ID	r²[population]
rs10780033	0.80[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs11130176	0.90[EUR][1000 genomes]
rs1134591	0.85[AFR][1000 genomes];0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs11705737	0.82[AMR][1000 genomes];0.97[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs11705888	0.83[EUR][1000 genomes]
rs11920534	0.95[EUR][1000 genomes]
rs11924597	0.86[AFR][1000 genomes];0.86[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs12491743	0.84[EUR][1000 genomes]
rs12493289	0.93[EUR][1000 genomes]
rs12637037	0.81[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs13064784	0.81[EUR][1000 genomes]
rs13064911	0.81[AFR][1000 genomes];0.93[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs13072911	0.81[AFR][1000 genomes];0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs13076394	0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs13078308	0.87[EUR][1000 genomes]
rs13090839	0.81[ASN][1000 genomes]
rs13315711	0.81[AFR][1000 genomes];0.91[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs13316620	0.80[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs28642807	0.84[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs3774628	0.82[EUR][1000 genomes]
rs4072859	0.84[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs4974079	0.93[EUR][1000 genomes]
rs4974080	0.83[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs4974082	0.82[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs4974084	0.85[AFR][1000 genomes];0.84[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs4974085	0.87[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs4974087	0.80[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs4974091	0.86[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs6414613	0.84[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs6446196	0.90[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs6446198	0.90[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs6446205	0.84[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs6446252	0.93[EUR][1000 genomes]
rs6446253	0.92[EUR][1000 genomes]
rs6768433	0.80[AFR][1000 genomes];0.89[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs6781790	0.86[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs6786665	0.90[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs6789285	0.91[EUR][1000 genomes]
rs6791234	0.82[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs6795025	0.82[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs7372149	0.82[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs7373778	0.89[EUR][1000 genomes]
rs7373790	0.89[EUR][1000 genomes]
rs7430198	0.90[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs7430501	0.80[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs7431710	0.95[EUR][1000 genomes]
rs7431857	0.80[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs7432989	0.85[EUR][1000 genomes]
rs7612459	0.84[AFR][1000 genomes];0.90[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs7615235	0.87[EUR][1000 genomes]
rs7615675	0.81[AFR][1000 genomes];0.87[AMR][1000 genomes];0.94[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs7621015	0.86[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs7623023	0.91[EUR][1000 genomes]
rs7626445	0.87[EUR][1000 genomes]
rs7627404	0.90[EUR][1000 genomes]
rs7628719	0.81[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs7636057	0.81[AFR][1000 genomes];0.90[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs7639332	0.84[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs7643368	0.80[AFR][1000 genomes];0.89[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs7647093	0.93[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs7649458	0.91[EUR][1000 genomes]
rs8926	0.84[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs9311430	0.90[EUR][1000 genomes]
rs9311432	0.90[EUR][1000 genomes]
rs9311433	0.90[EUR][1000 genomes]
rs9311434	0.91[EUR][1000 genomes]
rs9681717	0.93[EUR][1000 genomes]
rs9682444	0.90[EUR][1000 genomes]
rs9754878	0.93[EUR][1000 genomes]
rs9755490	0.93[EUR][1000 genomes]
rs9830636	0.88[EUR][1000 genomes]
rs9835307	0.90[EUR][1000 genomes]
rs9840050	0.82[EUR][1000 genomes]
rs9840684	0.93[EUR][1000 genomes]
rs9846123	0.90[EUR][1000 genomes]
rs9850134	0.89[AFR][1000 genomes];0.91[AMR][1000 genomes];0.98[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs9867373	0.89[AFR][1000 genomes];0.91[AMR][1000 genomes];0.98[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs9876848	0.90[EUR][1000 genomes]
rs9879971	0.80[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs9884022	0.89[AFR][1000 genomes];0.91[AMR][1000 genomes];0.98[EUR][1000 genomes];0.83[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3487342	chr3:48823957-48960475	Weak transcription Active TSS Strong transcription Flanking Active TSS Bivalent/Poised TSS Enhancers Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	39 gene(s)	inside rSNPs	diseases
2	esv3487343	chr3:48823963-48960381	Weak transcription Active TSS Enhancers Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	39 gene(s)	inside rSNPs	diseases
3	nsv980012	chr3:48935037-48963512	Strong transcription Flanking Active TSS Enhancers Weak transcription Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	30 gene(s)	inside rSNPs	diseases

mRNA abundance (count:24)

SNP	Gene	Cis/trans	Tissue	Source
rs13064883	WDR6	cis	Stomach	GTEx
rs13064883	AMT	cis	Muscle Skeletal	GTEx
rs13064883	WDR6	cis	Esophagus Muscularis	GTEx
rs13064883	WDR6	cis	Nerve Tibial	GTEx
rs13064883	PH-4	Cis_1M	lymphoblastoid	RTeQTL
rs13064883	AMT	cis	Thyroid	GTEx
rs13064883	WDR6	cis	Artery Tibial	GTEx
rs13064883	WDR6	cis	lung	GTEx
rs13064883	WDR6	cis	Adipose Subcutaneous	GTEx
rs13064883	NCKIPSD	cis	Esophagus Muscularis	GTEx
rs13064883	NCKIPSD	cis	Nerve Tibial	GTEx
rs13064883	NICN1-AS1	cis	Thyroid	GTEx
rs13064883	NCKIPSD	cis	Whole Blood	GTEx
rs13064883	ARIH2	Cis_1M	lymphoblastoid	RTeQTL
rs13064883	WDR6	cis	Esophagus Mucosa	GTEx
rs13064883	CCDC36	cis	Artery Tibial	GTEx
rs13064883	WDR6	cis	Muscle Skeletal	GTEx
rs13064883	WDR6	cis	Heart Left Ventricle	GTEx
rs13064883	CCDC36	cis	Esophagus Muscularis	GTEx
rs13064883	NICN1	cis	Thyroid	GTEx
rs13064883	ARIH2	cis	Thyroid	GTEx
rs13064883	WDR6	cis	Skin Sun Exposed Lower leg	GTEx
rs13064883	WDR6	cis	Whole Blood	GTEx
rs13064883	NCKIPSD	cis	Muscle Skeletal	GTEx

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:48936600-48954800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr3:48936600-48954800	Weak transcription	Sigmoid Colon	Sigmoid Colon
3	chr3:48942400-48954600	Weak transcription	Primary T helper cells fromperipheralblood	blood
4	chr3:48945800-48954800	Weak transcription	Fetal Muscle Leg	muscle
5	chr3:48950600-48954800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
6	chr3:48950800-48954800	Weak transcription	Brain Substantia Nigra	brain
7	chr3:48950800-48954800	Weak transcription	Fetal Brain Male	brain
8	chr3:48951600-48953000	Enhancers	HepG2	liver
9	chr3:48951600-48953600	Strong transcription	Fetal Thymus	thymus
10	chr3:48951600-48954800	Weak transcription	Fetal Stomach	stomach

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