Variant report

Variant	rs467364
Chromosome Location	chr21:16091904-16091905
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr21:16091185..16093425-chr21:16097360..16100309,2	MCF-7	breast:
2	chr21:16072697..16075664-chr21:16091482..16093697,2	K562	blood:
3	chr21:16090974..16093550-chr21:16099638..16101835,2	K562	blood:

Extended variants
information (count: 42 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:41)

rs_ID	r²[population]
rs1011868	0.93[ASN][1000 genomes]
rs1011869	0.93[ASN][1000 genomes]
rs11700788	0.93[ASN][1000 genomes]
rs11701060	0.93[ASN][1000 genomes]
rs11701668	0.93[ASN][1000 genomes]
rs11701709	0.85[ASN][1000 genomes]
rs11701752	0.93[ASN][1000 genomes]
rs11701758	0.93[ASN][1000 genomes]
rs11702307	0.81[AFR][1000 genomes];0.84[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs1292751	0.84[ASN][1000 genomes]
rs13046554	0.93[ASN][1000 genomes]
rs13049928	0.93[ASN][1000 genomes]
rs13050255	0.93[ASN][1000 genomes]
rs2007558	0.81[AFR][1000 genomes];0.82[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs2246699	0.81[AFR][1000 genomes]
rs2403804	0.84[ASN][1000 genomes]
rs2446696	0.81[AFR][1000 genomes];0.89[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs2822873	0.93[ASN][1000 genomes]
rs2822874	0.93[ASN][1000 genomes]
rs2822875	0.93[ASN][1000 genomes]
rs2822876	0.93[ASN][1000 genomes]
rs2822877	0.93[ASN][1000 genomes]
rs2822878	0.87[ASN][1000 genomes]
rs2822883	0.87[ASN][1000 genomes]
rs2822884	0.87[ASN][1000 genomes]
rs2822885	0.83[ASN][1000 genomes]
rs2822886	0.83[ASN][1000 genomes]
rs34595740	0.87[ASN][1000 genomes]
rs458052	0.84[EUR][1000 genomes]
rs460240	0.91[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs460246	0.86[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs62218099	0.93[ASN][1000 genomes]
rs62218100	0.81[AFR][1000 genomes];0.84[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs62218101	0.93[ASN][1000 genomes]
rs7280249	0.91[ASN][1000 genomes]
rs7280684	0.84[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs7281408	0.91[ASN][1000 genomes]
rs7281420	0.91[ASN][1000 genomes]
rs8130742	0.84[ASN][1000 genomes]
rs8132570	0.91[ASN][1000 genomes]
rs9983243	0.87[ASN][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv834045	chr21:15900678-16112850	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Genic enhancers Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr21:16091000-16092600	Enhancers	K562	blood

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