Variant report

Variant	rs67529975
Chromosome Location	chr4:63168556-63168557
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 37 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:27)

rs_ID	r²[population]
rs10014304	1.00[ASN][1000 genomes]
rs10517557	0.87[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs10517558	0.87[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs11131360	1.00[ASN][1000 genomes]
rs13108646	1.00[ASN][1000 genomes]
rs13109058	1.00[ASN][1000 genomes]
rs13111304	1.00[ASN][1000 genomes]
rs13118308	1.00[ASN][1000 genomes]
rs13123239	1.00[ASN][1000 genomes]
rs13125062	1.00[ASN][1000 genomes]
rs13131100	1.00[ASN][1000 genomes]
rs13143865	1.00[ASN][1000 genomes]
rs13149735	1.00[ASN][1000 genomes]
rs1350649	0.87[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs17828666	0.87[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs1870528	0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs33932625	0.93[AFR][1000 genomes];0.88[AMR][1000 genomes];0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34978365	1.00[ASN][1000 genomes]
rs4860455	1.00[ASN][1000 genomes]
rs4860459	1.00[ASN][1000 genomes]
rs56150500	1.00[ASN][1000 genomes]
rs62306419	1.00[ASN][1000 genomes]
rs6815671	1.00[ASN][1000 genomes]
rs6825910	1.00[ASN][1000 genomes]
rs6841045	1.00[ASN][1000 genomes]
rs72641216	1.00[ASN][1000 genomes]
rs9994443	1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:10 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1012093	chr4:63014592-63568580	Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	nsv537113	chr4:63014592-63568580	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
3	nsv534618	chr4:63025655-63568620	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
4	nsv997505	chr4:63025663-63575696	Enhancers Active TSS Weak transcription ZNF genes & repeats Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
5	nsv594333	chr4:63025823-63467034	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
6	nsv1013850	chr4:63049885-63568580	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
7	nsv537114	chr4:63049885-63568580	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
8	nsv594335	chr4:63054757-63183246	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	n/a
9	nsv879079	chr4:63059672-63184850	Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	n/a
10	nsv594336	chr4:63075414-63183246	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	n/a

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:63167200-63172400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links