Variant report

Variant	rs1602682
Chromosome Location	chr4:167355919-167355920
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 44 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:35)

rs_ID	r²[population]
rs10002331	0.92[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs10002718	0.92[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs1021431	0.82[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs11100650	0.92[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs12501155	0.92[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs13105316	0.92[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs13115190	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1352964	1.00[EUR][1000 genomes]
rs1352968	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1352969	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1492518	0.84[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1492539	0.96[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs1492541	0.96[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs1492542	0.92[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs1492544	0.92[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs1565652	0.87[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs1602678	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1602679	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1602681	0.97[EUR][1000 genomes]
rs1982867	0.94[EUR][1000 genomes]
rs2131246	1.00[AFR][1000 genomes]
rs2322566	0.92[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs2322567	0.92[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs2322808	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs28883115	1.00[EUR][1000 genomes]
rs3967162	0.91[EUR][1000 genomes]
rs4147009	0.91[EUR][1000 genomes]
rs4539997	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4543070	0.96[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs4691277	0.92[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs6817769	0.92[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs6841675	0.92[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs7667280	0.88[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs7671205	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9991895	0.92[AMR][1000 genomes];0.94[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1034421	chr4:166961339-167893289	Enhancers ZNF genes & repeats Weak transcription Active TSS Flanking Active TSS Strong transcription Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	nsv537339	chr4:166961339-167893289	Weak transcription Enhancers Flanking Active TSS Genic enhancers Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
3	nsv1032009	chr4:167154813-167403235	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
4	nsv880900	chr4:167155443-167368812	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS Strong transcription	TF binding region Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
5	nsv880967	chr4:167185391-167366567	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS Strong transcription	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
6	nsv881405	chr4:167193885-167628013	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
7	nsv1023051	chr4:167304814-168211540	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
8	nsv537340	chr4:167304814-168211540	Flanking Active TSS Enhancers ZNF genes & repeats Weak transcription Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
9	nsv1028788	chr4:167315021-167403235	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:12 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:167353600-167356400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr4:167354000-167356200	Weak transcription	Osteobl	bone
3	chr4:167354200-167356400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
4	chr4:167354600-167356400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
5	chr4:167355200-167357600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
6	chr4:167355200-167357600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
7	chr4:167355600-167356400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
8	chr4:167355600-167357200	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
9	chr4:167355800-167357400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
10	chr4:167355800-167357400	Enhancers	HUVEC	blood vessel
11	chr4:167355800-167358400	Enhancers	Muscle Satellite Cultured Cells	--
12	chr4:167355800-167358400	Enhancers	HMEC	breast

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