Variant report

Variant	rs615294
Chromosome Location	chr18:40374586-40374587
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 54 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:52)

rs_ID	r²[population]
rs11082297	0.97[ASN][1000 genomes]
rs11872616	0.97[ASN][1000 genomes]
rs11873248	0.98[ASN][1000 genomes]
rs11876135	0.98[ASN][1000 genomes]
rs12457018	0.99[ASN][1000 genomes]
rs1626483	0.97[ASN][1000 genomes]
rs1835500	0.97[ASN][1000 genomes]
rs1943171	0.97[ASN][1000 genomes]
rs1943177	0.97[ASN][1000 genomes]
rs1943178	0.97[ASN][1000 genomes]
rs1943179	0.98[ASN][1000 genomes]
rs2642799	0.87[AFR][1000 genomes];0.85[AMR][1000 genomes];0.88[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs28447520	0.97[ASN][1000 genomes]
rs28780768	0.94[ASN][1000 genomes]
rs476407	0.99[ASN][1000 genomes]
rs485404	0.99[ASN][1000 genomes]
rs488182	0.97[ASN][1000 genomes]
rs529072	0.99[ASN][1000 genomes]
rs559216	0.97[ASN][1000 genomes]
rs587697	0.97[ASN][1000 genomes]
rs589041	0.98[ASN][1000 genomes]
rs594272	0.98[ASN][1000 genomes]
rs597269	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs604330	0.99[ASN][1000 genomes]
rs604565	0.88[AFR][1000 genomes];0.85[AMR][1000 genomes];0.86[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs606128	0.97[ASN][1000 genomes]
rs60827299	0.98[ASN][1000 genomes]
rs615912	0.98[ASN][1000 genomes]
rs617272	0.98[ASN][1000 genomes]
rs621000	0.99[ASN][1000 genomes]
rs622364	0.84[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs633351	0.98[ASN][1000 genomes]
rs635930	0.97[ASN][1000 genomes]
rs646328	0.84[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs6507502	0.99[ASN][1000 genomes]
rs679462	0.99[ASN][1000 genomes]
rs7228468	0.91[ASN][1000 genomes]
rs7235419	0.97[ASN][1000 genomes]
rs7238151	0.99[ASN][1000 genomes]
rs7238693	0.99[ASN][1000 genomes]
rs7239233	0.99[ASN][1000 genomes]
rs7242948	0.94[ASN][1000 genomes]
rs8090510	0.99[ASN][1000 genomes]
rs8098030	0.99[ASN][1000 genomes]
rs8098429	0.97[ASN][1000 genomes]
rs8099760	0.99[ASN][1000 genomes]
rs9946696	0.99[ASN][1000 genomes]
rs9947110	0.99[ASN][1000 genomes]
rs9947132	0.99[ASN][1000 genomes]
rs9953581	0.97[ASN][1000 genomes]
rs9961268	0.97[ASN][1000 genomes]
rs9967226	0.97[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv833632	chr18:40187679-40388058	Flanking Active TSS Weak transcription Active TSS Enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
2	nsv1056794	chr18:40197837-40688514	Flanking Active TSS Enhancers Weak transcription Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	5 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	chr18:40373400-40374800	Enhancers	iPS-18 Cell Line	embryonic stem cell
2	chr18:40374200-40378600	Weak transcription	H1 Cell Line	embryonic stem cell

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links