Variant report

Variant	rs10496713
Chromosome Location	chr2:134546481-134546482
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 34 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:30)

rs_ID	r²[population]
rs10184200	0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11884849	0.96[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs11888079	0.96[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs12691846	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12989210	0.81[EUR][1000 genomes]
rs12993296	0.91[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs12995146	0.97[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs12996062	0.82[ASN][1000 genomes]
rs12996450	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12996471	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13002440	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13006611	0.80[AFR][1000 genomes];0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs13011121	0.94[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs13013221	0.94[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs13015979	0.96[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs13017617	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13032020	0.82[ASN][1000 genomes]
rs13032581	0.81[AMR][1000 genomes];0.97[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs13033059	0.96[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs13036190	0.82[ASN][1000 genomes]
rs1374405	0.82[ASN][1000 genomes]
rs1446752	0.94[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs1562348	0.82[ASN][1000 genomes]
rs1867897	0.96[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs35961497	0.82[ASN][1000 genomes]
rs4536693	0.90[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs62166122	0.81[EUR][1000 genomes]
rs62166124	0.82[AFR][1000 genomes];0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7568496	0.96[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs9917166	0.96[EUR][1000 genomes];0.82[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1003624	chr2:134126928-134583203	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
2	nsv1006101	chr2:134263288-134973917	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	14 gene(s)	inside rSNPs	diseases
3	nsv1013713	chr2:134322236-134644574	Enhancers Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
4	nsv535931	chr2:134322236-134644574	Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription Active TSS Flanking Bivalent TSS/Enh Genic enhancers Strong transcription ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs10496713	MZT2B	cis	parietal	SCAN

Chromatin state (count:16 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:134538200-134547600	Weak transcription	Fetal Heart	heart
2	chr2:134542800-134547600	Weak transcription	HUVEC	blood vessel
3	chr2:134544000-134549400	Enhancers	Osteobl	bone
4	chr2:134544600-134546600	Enhancers	Muscle Satellite Cultured Cells	--
5	chr2:134544600-134546600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
6	chr2:134544600-134546800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
7	chr2:134544600-134549600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
8	chr2:134544600-134549800	Enhancers	NHDF-Ad	bronchial
9	chr2:134544800-134546800	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
10	chr2:134544800-134549600	Enhancers	NHLF	lung
11	chr2:134545000-134557000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
12	chr2:134546000-134547200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
13	chr2:134546000-134547400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
14	chr2:134546200-134548200	Weak transcription	NH-A	brain
15	chr2:134546200-134548400	Weak transcription	HSMM	muscle
16	chr2:134546400-134548800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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