Variant report

Variant	rs9354800
Chromosome Location	chr6:69499415-69499416
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 53 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:49)

rs_ID	r²[population]
rs1015152	0.91[ASN][1000 genomes]
rs11965496	0.92[ASN][1000 genomes]
rs1357618	0.83[ASN][1000 genomes]
rs1357619	0.92[ASN][1000 genomes]
rs1403927	0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1523937	0.92[ASN][1000 genomes]
rs1523941	0.86[ASN][1000 genomes]
rs1523947	0.86[ASN][1000 genomes]
rs1523948	0.92[ASN][1000 genomes]
rs2140510	0.92[ASN][1000 genomes]
rs2140511	0.92[ASN][1000 genomes]
rs2177448	0.92[ASN][1000 genomes]
rs2204285	0.94[ASN][1000 genomes]
rs2206834	0.94[ASN][1000 genomes]
rs2223724	0.94[ASN][1000 genomes]
rs6455299	0.89[ASN][1000 genomes]
rs6455302	0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6455303	0.92[ASN][1000 genomes]
rs6903692	0.85[ASN][1000 genomes]
rs6907661	0.92[ASN][1000 genomes]
rs6911395	0.92[ASN][1000 genomes]
rs6919103	0.92[ASN][1000 genomes]
rs6920537	0.92[ASN][1000 genomes]
rs6924533	0.83[ASN][1000 genomes]
rs6929378	0.94[ASN][1000 genomes]
rs7751539	0.94[ASN][1000 genomes]
rs7755356	0.94[ASN][1000 genomes]
rs7758017	0.92[ASN][1000 genomes]
rs7765583	0.91[ASN][1000 genomes]
rs7769724	0.94[ASN][1000 genomes]
rs7771494	0.83[ASN][1000 genomes]
rs7775093	0.92[ASN][1000 genomes]
rs9294807	0.94[ASN][1000 genomes]
rs9294810	0.92[ASN][1000 genomes]
rs9294811	0.91[ASN][1000 genomes]
rs9346239	0.82[AMR][1000 genomes];0.95[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs9346240	0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs9346241	0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs9346243	0.90[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs9346245	0.92[AFR][1000 genomes];0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs9346246	0.91[ASN][1000 genomes]
rs9360360	0.86[ASN][1000 genomes]
rs9360361	0.92[ASN][1000 genomes]
rs9446057	0.92[ASN][1000 genomes]
rs9446058	0.94[ASN][1000 genomes]
rs9454616	0.94[ASN][1000 genomes]
rs9454621	0.92[ASN][1000 genomes]
rs9454622	0.92[ASN][1000 genomes]
rs992784	0.92[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv886130	chr6:68950298-69531957	Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Bivalent Enhancer Bivalent/Poised TSS Active TSS Genic enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
2	nsv886131	chr6:69480628-69545903	Weak transcription Active TSS Flanking Active TSS Enhancers Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
3	nsv886132	chr6:69487204-69610281	Enhancers ZNF genes & repeats Weak transcription Active TSS Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer	Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
4	nsv1017659	chr6:69489481-69520127	Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region	2 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	chr6:69489600-69507000	Weak transcription	Fetal Lung	lung
2	chr6:69499400-69499800	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell

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