Variant report

Variant	rs56282499
Chromosome Location	chr2:183049555-183049556
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 77 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:75)

rs_ID	r²[population]
rs10201929	0.93[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs10202082	0.90[EUR][1000 genomes]
rs10930994	0.95[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs13034133	0.95[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs1344773	0.88[AMR][1000 genomes];0.98[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs1347079	0.82[AMR][1000 genomes];0.96[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs1432517	0.95[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs1432518	0.94[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs1432519	0.87[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs1432520	0.96[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs1432521	0.95[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs1432533	0.83[AMR][1000 genomes];0.96[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs1594614	0.94[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs17366198	0.91[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs17366503	0.88[AMR][1000 genomes];0.98[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs17457164	0.94[AMR][1000 genomes];0.91[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs17457303	0.89[AMR][1000 genomes];0.88[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs17457323	0.91[AMR][1000 genomes];0.89[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs17595927	0.91[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs1835880	0.82[AMR][1000 genomes];0.96[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs1835881	0.94[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs1864847	0.96[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs1864848	0.94[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs1864849	0.95[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs1864850	0.95[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs1864851	0.88[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs1864852	0.95[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs1864854	0.91[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs1988750	0.90[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2116636	0.82[AMR][1000 genomes];0.92[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2128045	0.96[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2128046	0.96[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2128047	0.96[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2170402	0.95[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2170403	0.96[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2195880	0.89[AMR][1000 genomes];0.95[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2217614	0.84[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs2276612	0.95[AMR][1000 genomes];0.91[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2368255	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2368276	0.95[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2568660	0.82[AMR][1000 genomes];0.94[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2568661	0.96[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2568663	0.80[AMR][1000 genomes];0.95[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2568664	0.96[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2568667	0.96[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2568670	0.90[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2568672	0.94[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2568673	0.94[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2568674	0.94[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2568676	0.95[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2568682	0.81[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2568687	0.83[EUR][1000 genomes]
rs2623418	0.95[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2623422	0.84[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs2623423	0.84[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs2623435	0.96[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2623437	0.96[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs300885	0.83[EUR][1000 genomes]
rs3754929	0.95[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs4503956	0.96[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs4666819	0.89[AMR][1000 genomes];0.94[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs55747252	0.91[AMR][1000 genomes];0.99[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs56301405	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs57801137	0.86[AMR][1000 genomes];0.97[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6740401	0.96[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs68189385	0.80[AMR][1000 genomes];0.82[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs711808	0.83[EUR][1000 genomes]
rs72895040	0.95[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs753289	0.81[EUR][1000 genomes]
rs7571503	0.95[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs7581170	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs833133	0.81[EUR][1000 genomes]
rs833135	0.81[EUR][1000 genomes]
rs964757	0.91[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs964758	0.91[EUR][1000 genomes];0.84[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	nsv875477	chr2:182938377-183086478	Weak transcription Enhancers Strong transcription Active TSS ZNF genes & repeats Genic enhancers Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	nsv583913	chr2:183043563-183243313	ZNF genes & repeats Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:183047200-183049800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
2	chr2:183048200-183050400	Weak transcription	Colon Smooth Muscle	Colon
3	chr2:183048400-183049800	Weak transcription	Aorta	Aorta
4	chr2:183048400-183073000	Weak transcription	Fetal Stomach	stomach
5	chr2:183048800-183051000	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
6	chr2:183048800-183052000	Weak transcription	Fetal Intestine Large	intestine
7	chr2:183048800-183060000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
8	chr2:183049000-183050600	Strong transcription	Duodenum Smooth Muscle	Duodenum
9	chr2:183049400-183049800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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