Variant report

Variant	rs1075065
Chromosome Location	chr4:55867218-55867219
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 47 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:44)

rs_ID	r²[population]
rs11941928	0.92[ASN][1000 genomes]
rs12502309	0.92[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12640896	0.93[AFR][1000 genomes];0.93[AMR][1000 genomes];0.85[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs13101326	0.99[ASN][1000 genomes]
rs13101685	0.99[ASN][1000 genomes]
rs13101777	0.98[ASN][1000 genomes]
rs13104623	0.81[CEU][hapmap];0.98[ASN][1000 genomes]
rs13106311	0.98[ASN][1000 genomes]
rs13110915	0.99[ASN][1000 genomes]
rs13111813	0.98[ASN][1000 genomes]
rs13111838	0.96[ASN][1000 genomes]
rs13114647	0.97[ASN][1000 genomes]
rs13125964	0.89[AMR][1000 genomes];0.83[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs13126022	0.96[ASN][1000 genomes]
rs13126236	0.83[AMR][1000 genomes];0.85[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs13127180	0.98[ASN][1000 genomes]
rs13127753	0.98[ASN][1000 genomes]
rs13129153	0.98[ASN][1000 genomes]
rs13130324	0.94[ASN][1000 genomes]
rs13138898	0.98[ASN][1000 genomes]
rs13144612	0.98[ASN][1000 genomes]
rs13146834	0.98[ASN][1000 genomes]
rs4259115	0.98[ASN][1000 genomes]
rs4317261	0.98[ASN][1000 genomes]
rs4320192	0.98[ASN][1000 genomes]
rs4334808	0.98[ASN][1000 genomes]
rs4336286	0.98[ASN][1000 genomes]
rs4337782	0.98[ASN][1000 genomes]
rs4356964	0.89[AMR][1000 genomes];0.85[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4524450	0.98[ASN][1000 genomes]
rs4569809	0.97[ASN][1000 genomes]
rs4599477	0.97[ASN][1000 genomes]
rs61696777	0.98[ASN][1000 genomes]
rs6554219	0.97[ASN][1000 genomes]
rs6554222	0.98[ASN][1000 genomes]
rs6554223	0.98[ASN][1000 genomes]
rs6820549	0.98[ASN][1000 genomes]
rs6821744	0.98[ASN][1000 genomes]
rs6822352	0.93[ASN][1000 genomes]
rs6824426	0.94[ASN][1000 genomes]
rs6826834	0.98[ASN][1000 genomes]
rs71624987	0.98[ASN][1000 genomes]
rs7657044	0.98[ASN][1000 genomes]
rs7667898	0.97[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv526344	chr4:55522488-56231119	Weak transcription Enhancers Active TSS Bivalent Enhancer Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	25 gene(s)	inside rSNPs	diseases
2	nsv948758	chr4:55748430-55887962	Enhancers Flanking Active TSS Active TSS Weak transcription Genic enhancers ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	nsv829939	chr4:55856771-56005011	Enhancers Flanking Bivalent TSS/Enh Genic enhancers Weak transcription Strong transcription Flanking Active TSS Bivalent/Poised TSS Active TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:55865800-55870600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
2	chr4:55865800-55870600	Weak transcription	Adipose Nuclei	Adipose

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