Variant report

Variant	rs2365191
Chromosome Location	chr2:31258266-31258267
allele	C/T
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:52)

rs_ID	r²[population]
rs10164479	0.93[ASN][1000 genomes]
rs10166921	0.94[ASN][1000 genomes]
rs10174368	0.93[ASN][1000 genomes]
rs10192472	0.91[ASN][1000 genomes]
rs10197865	0.94[ASN][1000 genomes]
rs10206704	0.89[ASN][1000 genomes]
rs10209881	0.94[ASN][1000 genomes]
rs10210092	0.94[ASN][1000 genomes]
rs10210124	0.85[ASN][1000 genomes]
rs10210300	0.93[ASN][1000 genomes]
rs10865086	0.95[ASN][1000 genomes]
rs12473730	0.93[ASN][1000 genomes]
rs12712300	0.94[ASN][1000 genomes]
rs1862964	0.95[ASN][1000 genomes]
rs1862965	0.95[ASN][1000 genomes]
rs1862966	0.96[ASN][1000 genomes]
rs1862967	0.96[ASN][1000 genomes]
rs1862968	0.96[ASN][1000 genomes]
rs2113487	0.95[ASN][1000 genomes]
rs2113488	0.95[ASN][1000 genomes]
rs2161835	0.91[ASN][1000 genomes]
rs2194454	0.93[ASN][1000 genomes]
rs2194456	0.93[ASN][1000 genomes]
rs2194457	0.90[ASN][1000 genomes]
rs2216827	0.85[ASN][1000 genomes]
rs4951959	0.90[ASN][1000 genomes]
rs4952027	0.86[ASN][1000 genomes]
rs4952028	0.90[ASN][1000 genomes]
rs4952030	0.94[ASN][1000 genomes]
rs4952031	0.89[ASN][1000 genomes]
rs4952032	0.92[ASN][1000 genomes]
rs4952033	0.84[ASN][1000 genomes]
rs4952038	0.80[ASN][1000 genomes]
rs5009910	0.93[ASN][1000 genomes]
rs56284247	0.82[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs62140629	0.83[ASN][1000 genomes]
rs6543594	0.86[ASN][1000 genomes]
rs6543595	0.90[ASN][1000 genomes]
rs6708989	0.93[ASN][1000 genomes]
rs6752071	0.92[ASN][1000 genomes]
rs6752303	0.93[ASN][1000 genomes]
rs6752662	0.93[ASN][1000 genomes]
rs7558425	0.93[ASN][1000 genomes]
rs7565923	0.90[ASN][1000 genomes]
rs7579017	0.89[ASN][1000 genomes]
rs7582401	0.95[ASN][1000 genomes]
rs7592553	0.89[ASN][1000 genomes]
rs7601904	0.86[ASN][1000 genomes]
rs7605643	0.95[ASN][1000 genomes]
rs7608731	0.93[ASN][1000 genomes]
rs9308914	0.89[ASN][1000 genomes]
rs9679162	0.93[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	nsv948552	chr2:31118599-31595424	Flanking Active TSS Weak transcription Enhancers Strong transcription Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:31246400-31261600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
2	chr2:31251400-31270000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr2:31257800-31259600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr2:31258000-31258800	Weak transcription	Primary neutrophils fromperipheralblood	blood

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links