Variant report

Variant	rs895105
Chromosome Location	chr4:95911893-95911894
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 58 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:52)

rs_ID	r²[population]
rs11097454	0.90[ASN][1000 genomes]
rs1160695	0.87[ASN][1000 genomes]
rs12507710	0.81[ASN][1000 genomes]
rs13128586	0.83[ASN][1000 genomes]
rs13129054	0.83[ASN][1000 genomes]
rs13129062	0.90[ASN][1000 genomes]
rs13145631	0.81[ASN][1000 genomes]
rs1347346	0.90[ASN][1000 genomes]
rs1434546	0.83[ASN][1000 genomes]
rs1444920	0.90[ASN][1000 genomes]
rs1444921	0.90[ASN][1000 genomes]
rs1444926	0.87[ASN][1000 genomes]
rs1470409	0.87[ASN][1000 genomes]
rs1530459	0.81[ASN][1000 genomes]
rs1545326	0.83[ASN][1000 genomes]
rs1545327	0.87[ASN][1000 genomes]
rs1545329	0.90[ASN][1000 genomes]
rs1821451	0.87[ASN][1000 genomes]
rs1822826	0.87[ASN][1000 genomes]
rs1834718	0.83[ASN][1000 genomes]
rs1838501	0.87[ASN][1000 genomes]
rs1867542	0.90[ASN][1000 genomes]
rs2044328	0.85[ASN][1000 genomes]
rs2120832	0.90[ASN][1000 genomes]
rs3755874	0.81[ASN][1000 genomes]
rs3775034	0.83[ASN][1000 genomes]
rs4145993	0.87[ASN][1000 genomes]
rs4331783	0.87[ASN][1000 genomes]
rs4397000	0.87[ASN][1000 genomes]
rs4450936	0.90[ASN][1000 genomes]
rs4588466	0.90[ASN][1000 genomes]
rs4699827	0.90[ASN][1000 genomes]
rs4699828	0.90[ASN][1000 genomes]
rs6532520	0.81[ASN][1000 genomes]
rs6532523	0.83[ASN][1000 genomes]
rs6815448	0.90[ASN][1000 genomes]
rs6816059	0.90[ASN][1000 genomes]
rs6820199	0.87[ASN][1000 genomes]
rs6836504	0.90[ASN][1000 genomes]
rs6840826	0.87[ASN][1000 genomes]
rs6841746	0.90[ASN][1000 genomes]
rs6843668	0.90[ASN][1000 genomes]
rs6844029	0.87[ASN][1000 genomes]
rs6853845	0.87[ASN][1000 genomes]
rs6855395	0.87[ASN][1000 genomes]
rs716190	0.90[ASN][1000 genomes]
rs7698787	0.90[ASN][1000 genomes]
rs920911	0.81[ASN][1000 genomes]
rs920912	0.81[ASN][1000 genomes]
rs965447	0.87[ASN][1000 genomes]
rs973887	0.90[ASN][1000 genomes]
rs996659	0.90[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv932216	chr4:95501261-96109807	Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Genic enhancers Strong transcription Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
2	nsv1003860	chr4:95507683-96120619	Weak transcription Enhancers Strong transcription Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
3	nsv869528	chr4:95537649-96368018	Weak transcription Enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Active TSS Strong transcription Genic enhancers Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
4	nsv492312	chr4:95823124-96128327	Flanking Active TSS Weak transcription Enhancers Active TSS Strong transcription 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 miRNA target site	2 gene(s)	inside rSNPs	diseases
5	nsv997787	chr4:95859839-95934105	Enhancers Flanking Active TSS Active TSS Weak transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
6	nsv537190	chr4:95859839-95934105	Enhancers Weak transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:95908800-95915400	Weak transcription	A549	lung

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