Variant report

Variant	rs6832298
Chromosome Location	chr4:90072325-90072326
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 56 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:50)

rs_ID	r²[population]
rs10025332	0.98[AFR][1000 genomes];0.99[ASN][1000 genomes]
rs10516828	0.92[ASN][1000 genomes]
rs12507349	0.92[ASN][1000 genomes]
rs1398945	0.92[ASN][1000 genomes]
rs1513817	0.90[AFR][1000 genomes]
rs17015025	0.84[ASN][1000 genomes]
rs17770293	0.86[ASN][1000 genomes]
rs1996140	0.87[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs2280099	0.84[ASN][1000 genomes]
rs3822085	0.84[ASN][1000 genomes]
rs55806245	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs55996516	0.93[ASN][1000 genomes]
rs56111951	0.92[ASN][1000 genomes]
rs56147277	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56165603	0.84[ASN][1000 genomes]
rs56344658	0.92[ASN][1000 genomes]
rs56355329	0.92[ASN][1000 genomes]
rs61082288	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61295522	0.87[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs62306393	0.86[ASN][1000 genomes]
rs6825767	0.93[AFR][1000 genomes];0.99[ASN][1000 genomes]
rs6825804	0.98[AFR][1000 genomes];0.99[ASN][1000 genomes]
rs6826021	0.92[AFR][1000 genomes]
rs6826703	0.97[AFR][1000 genomes];0.98[ASN][1000 genomes]
rs6826754	0.81[AFR][1000 genomes]
rs72668152	0.84[ASN][1000 genomes]
rs72668154	0.84[ASN][1000 genomes]
rs72668156	0.84[ASN][1000 genomes]
rs72668157	0.84[ASN][1000 genomes]
rs72668165	0.84[ASN][1000 genomes]
rs72668167	0.84[ASN][1000 genomes]
rs72668171	0.84[ASN][1000 genomes]
rs72668179	0.86[ASN][1000 genomes]
rs72668183	0.93[ASN][1000 genomes]
rs72668187	0.92[ASN][1000 genomes]
rs72668189	0.92[ASN][1000 genomes]
rs72668192	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72668193	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72668195	0.98[AFR][1000 genomes];0.99[ASN][1000 genomes]
rs72668196	0.98[AFR][1000 genomes];0.99[ASN][1000 genomes]
rs72670003	0.97[AFR][1000 genomes];0.99[ASN][1000 genomes]
rs72670004	0.87[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs72670005	0.87[EUR][1000 genomes]
rs72670006	0.87[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs72670007	0.81[ASN][1000 genomes]
rs756227	0.98[AFR][1000 genomes];0.99[ASN][1000 genomes]
rs7660709	0.85[ASN][1000 genomes]
rs7669140	0.86[ASN][1000 genomes]
rs7697393	0.92[AFR][1000 genomes]
rs8582	0.84[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	nsv470051	chr4:89644931-90643144	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
2	nsv1007025	chr4:89837734-90098046	Enhancers Flanking Active TSS Strong transcription Active TSS Weak transcription ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
3	nsv537176	chr4:89837734-90098046	Weak transcription Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer 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	nsv1002448	chr4:89933385-90128133	Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Genic enhancers Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
5	nsv470052	chr4:90055898-90075384	Weak transcription ZNF genes & repeats Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
6	nsv830002	chr4:90056232-90258865	Weak transcription Active TSS Enhancers Flanking Active TSS Strong transcription Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 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	chr4:90070200-90079000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links