Variant report

Variant	rs6813390
Chromosome Location	chr4:149241207-149241208
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 32 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:25)

rs_ID	r²[population]
rs10024999	0.80[ASN][1000 genomes]
rs12499873	0.80[ASN][1000 genomes]
rs12499901	0.80[ASN][1000 genomes]
rs12508913	0.80[ASN][1000 genomes]
rs12511415	0.82[ASN][1000 genomes]
rs12647673	0.80[ASN][1000 genomes]
rs13116551	0.80[ASN][1000 genomes]
rs1818448	0.80[ASN][1000 genomes]
rs2048548	0.80[ASN][1000 genomes]
rs28379421	0.80[ASN][1000 genomes]
rs28607266	0.80[ASN][1000 genomes]
rs28645256	0.80[ASN][1000 genomes]
rs3920217	0.80[ASN][1000 genomes]
rs55649367	0.80[ASN][1000 genomes]
rs58464129	0.80[ASN][1000 genomes]
rs62333584	0.80[ASN][1000 genomes]
rs6535602	0.80[ASN][1000 genomes]
rs6819635	0.80[ASN][1000 genomes]
rs6832421	0.80[ASN][1000 genomes]
rs6840141	0.80[ASN][1000 genomes]
rs6842079	0.80[ASN][1000 genomes]
rs6849127	0.80[ASN][1000 genomes]
rs6849327	0.80[ASN][1000 genomes]
rs6849862	0.80[ASN][1000 genomes]
rs7688209	0.80[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1027263	chr4:149127120-149320135	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
2	nsv537296	chr4:149127120-149320135	Flanking Active TSS Weak transcription Enhancers Active TSS ZNF genes & repeats Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
3	nsv1031815	chr4:149172485-149282928	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
4	nsv1028105	chr4:149199913-149284620	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Strong transcription	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
5	nsv537297	chr4:149199913-149284620	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Strong transcription	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
6	nsv1016966	chr4:149209467-149341037	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
7	nsv1019350	chr4:149232430-149282117	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:149235000-149266800	Weak transcription	Rectal Mucosa Donor 31	rectum
2	chr4:149237000-149249600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
3	chr4:149237800-149246200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood

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