Variant report

Variant	rs4563285
Chromosome Location	chr2:46669944-46669945
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr2:46633572..46635870-chr2:46669679..46671465,2	MCF-7	breast:
2	chr2:46541786..46543916-chr2:46667813..46670793,2	K562	blood:
3	chr2:46668595..46671087-chr2:46674345..46676657,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000241791	Chromatin interaction

Extended variants
information (count: 48 )
Associated
traits (count: 2 )

rSNPs within LD-proxies of this variant (count:36)

rs_ID	r²[population]
rs11125075	0.96[ASN][1000 genomes]
rs12986899	0.82[AMR][1000 genomes];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12991646	0.89[ASN][1000 genomes]
rs13002880	0.80[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs13003074	0.96[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13010062	0.91[ASN][1000 genomes]
rs13020043	0.80[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs13024414	0.86[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs1530621	0.87[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs1530624	0.90[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1530628	0.82[EUR][1000 genomes]
rs1597040	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs1900591	0.82[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs2121698	0.92[EUR][1000 genomes]
rs2121700	0.91[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs34712412	0.89[ASN][1000 genomes]
rs34791442	0.91[ASN][1000 genomes]
rs34854267	0.91[EUR][1000 genomes]
rs35462976	0.85[ASN][1000 genomes]
rs35509718	0.80[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs36006825	0.91[EUR][1000 genomes]
rs4312543	0.80[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs4396767	0.90[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4549147	0.89[EUR][1000 genomes]
rs4953365	0.89[ASN][1000 genomes]
rs4953371	0.87[ASN][1000 genomes]
rs4953372	0.89[ASN][1000 genomes]
rs4953377	0.82[EUR][1000 genomes]
rs4953379	0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56048837	0.96[ASN][1000 genomes]
rs6544895	0.80[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs6718875	0.87[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs6749877	0.80[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs6757564	0.90[EUR][1000 genomes]
rs718849	0.80[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs7565188	0.88[EUR][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	nsv1012446	chr2:45921682-46737036	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	62 gene(s)	inside rSNPs	diseases
2	esv2757795	chr2:46532812-46874151	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	52 gene(s)	inside rSNPs	diseases
3	esv2759046	chr2:46532812-46874151	Active TSS Enhancers Flanking Active TSS Strong transcription Weak transcription Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	52 gene(s)	inside rSNPs	diseases
4	esv34650	chr2:46605659-46818992	Enhancers Weak transcription ZNF genes & repeats Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	38 gene(s)	inside rSNPs	diseases
5	esv2756919	chr2:46614235-46756431	Weak transcription Enhancers Flanking Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS Active TSS Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	35 gene(s)	inside rSNPs	diseases
6	nsv437435	chr2:46636967-46763587	Active TSS Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	33 gene(s)	inside rSNPs	diseases
7	nsv1001902	chr2:46651624-46675665	Enhancers Weak transcription Bivalent Enhancer Genic enhancers Active TSS ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	25 gene(s)	inside rSNPs	diseases
8	nsv997637	chr2:46651624-46676628	Bivalent Enhancer Enhancers Weak transcription Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Active TSS Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	25 gene(s)	inside rSNPs	diseases
9	nsv1003646	chr2:46651624-46677186	Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	25 gene(s)	inside rSNPs	diseases
10	esv34937	chr2:46651624-46818586	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS Bivalent Enhancer ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	36 gene(s)	inside rSNPs	diseases
11	nsv581745	chr2:46660445-46693963	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
12	nsv9702	chr2:46668106-46745740	Enhancers Active TSS Weak transcription Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases

mRNA abundance (count:2)

SNP	Gene	Cis/trans	Tissue	Source
rs4563285	ATP6V1E2	cis	Muscle Skeletal	GTEx
rs4563285	ATP6V1E2	cis	Heart Left Ventricle	GTEx

Chromatin state (count:11 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:46657200-46672200	Enhancers	HepG2	liver
2	chr2:46662200-46678400	Weak transcription	Placenta	Placenta
3	chr2:46663200-46671400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
4	chr2:46667000-46688400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr2:46668000-46670000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
6	chr2:46668000-46670600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
7	chr2:46668200-46683600	Weak transcription	K562	blood
8	chr2:46669600-46670000	Enhancers	Gastric	stomach
9	chr2:46669600-46670200	Enhancers	Pancreas	Pancrea
10	chr2:46669600-46671400	Enhancers	Breast Myoepithelial Primary Cells	Breast
11	chr2:46669800-46670200	Enhancers	Esophagus	oesophagus

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