Variant report

Variant	rs4594964
Chromosome Location	chr6:150792522-150792523
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 19 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:16)

rs_ID	r²[population]
rs1033446	0.83[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs11752980	0.88[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs11754755	0.84[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs35512316	0.85[AMR][1000 genomes]
rs60000576	0.84[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs67032163	0.88[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs6904218	0.91[MEX][hapmap]
rs7753910	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9371450	0.80[ASN][1000 genomes]
rs9372050	0.81[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs9383824	0.92[ASN][1000 genomes]
rs9383825	0.84[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs9383827	0.81[AMR][1000 genomes]
rs9384535	0.88[ASN][1000 genomes]
rs9480453	0.81[ASN][1000 genomes]
rs9480461	0.98[AFR][1000 genomes];0.99[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[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	nsv1020067	chr6:150730783-150870708	Enhancers Flanking Active TSS Weak transcription Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
2	nsv886772	chr6:150743364-151024280	Enhancers Active TSS Weak transcription Strong transcription Bivalent Enhancer Bivalent/Poised TSS Flanking 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	5 gene(s)	inside rSNPs	diseases
3	nsv886773	chr6:150751951-150799803	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:150787600-150792600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

Quick Search:

Input of quick search could be:

dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

what's new

Quick links