Variant report

Variant	rs56390006
Chromosome Location	chr2:52618489-52618490
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 55 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:43)

rs_ID	r²[population]
rs12991278	1.00[ASN][1000 genomes]
rs12999799	1.00[ASN][1000 genomes]
rs12999852	1.00[ASN][1000 genomes]
rs13005607	1.00[ASN][1000 genomes]
rs13006867	1.00[ASN][1000 genomes]
rs13012043	1.00[ASN][1000 genomes]
rs13013842	0.85[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs13013911	1.00[ASN][1000 genomes]
rs13016079	1.00[ASN][1000 genomes]
rs13017636	1.00[ASN][1000 genomes]
rs13018183	1.00[ASN][1000 genomes]
rs13019134	1.00[ASN][1000 genomes]
rs13020890	0.80[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs13033584	0.80[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs13417515	1.00[ASN][1000 genomes]
rs1364575	1.00[ASN][1000 genomes]
rs1364583	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1424802	1.00[ASN][1000 genomes]
rs2222686	0.80[AMR][1000 genomes];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34219622	0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34793475	1.00[ASN][1000 genomes]
rs34868438	1.00[ASN][1000 genomes]
rs35054050	1.00[ASN][1000 genomes]
rs35695189	1.00[ASN][1000 genomes]
rs35721673	1.00[ASN][1000 genomes]
rs35872223	1.00[ASN][1000 genomes]
rs4522646	1.00[ASN][1000 genomes]
rs4971594	0.85[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4971595	0.88[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs55648425	1.00[ASN][1000 genomes]
rs55855257	1.00[ASN][1000 genomes]
rs55962941	1.00[ASN][1000 genomes]
rs56314551	1.00[ASN][1000 genomes]
rs56333115	1.00[ASN][1000 genomes]
rs56383411	0.80[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs71411584	1.00[ASN][1000 genomes]
rs71411585	1.00[ASN][1000 genomes]
rs71411587	1.00[ASN][1000 genomes]
rs71411588	1.00[ASN][1000 genomes]
rs71411589	1.00[ASN][1000 genomes]
rs941055	0.80[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs941056	1.00[ASN][1000 genomes]
rs941057	1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:12 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1009513	chr2:51890060-52821980	ZNF genes & repeats Enhancers Weak transcription Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
2	nsv1007633	chr2:52217555-52862389	Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Active TSS Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
3	nsv535714	chr2:52217555-52862389	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
4	nsv874111	chr2:52383698-52962055	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	13 gene(s)	inside rSNPs	diseases
5	nsv1014619	chr2:52496317-52821980	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
6	nsv535717	chr2:52496317-52821980	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Genic enhancers Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
7	nsv834025	chr2:52514959-52693049	Enhancers Active TSS Weak transcription Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
8	nsv874114	chr2:52521126-52628235	Flanking Active TSS Enhancers Weak transcription Strong transcription Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
9	nsv998227	chr2:52527889-52821980	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Active TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
10	nsv581928	chr2:52572167-52656594	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Strong transcription Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
11	nsv874116	chr2:52582766-52685592	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
12	nsv581929	chr2:52599360-52761239	Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:52613800-52618800	Weak transcription	Fetal Brain Female	brain
2	chr2:52616800-52619000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
3	chr2:52617600-52619600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
4	chr2:52617800-52620600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr2:52618200-52618600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
6	chr2:52618200-52622200	Weak transcription	Osteobl	bone

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