Variant report

Variant	rs1585384
Chromosome Location	chr3:67790460-67790461
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 40 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:37)

rs_ID	r²[population]
rs10428091	0.95[ASN][1000 genomes]
rs10428122	0.96[ASN][1000 genomes]
rs11127733	0.90[AFR][1000 genomes];0.91[AMR][1000 genomes];0.92[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs12330732	0.87[AFR][1000 genomes];0.84[ASN][1000 genomes]
rs13067333	0.83[AMR][1000 genomes];0.92[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1459912	0.83[AFR][1000 genomes];0.92[ASN][1000 genomes]
rs1459913	0.94[AFR][1000 genomes];0.94[AMR][1000 genomes];0.91[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1459918	0.92[AFR][1000 genomes];0.91[ASN][1000 genomes]
rs1459919	0.95[AFR][1000 genomes];0.91[ASN][1000 genomes]
rs1599209	0.94[AFR][1000 genomes];0.96[AMR][1000 genomes];0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2125810	0.83[AFR][1000 genomes];0.93[ASN][1000 genomes]
rs2125812	0.91[AMR][1000 genomes];0.92[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2125813	0.90[AFR][1000 genomes];0.91[AMR][1000 genomes];0.92[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2169110	0.92[AFR][1000 genomes];0.87[AMR][1000 genomes];0.91[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2169111	0.95[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2169113	0.92[AFR][1000 genomes];0.91[AMR][1000 genomes];0.93[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2362440	0.94[AFR][1000 genomes];0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2362449	0.90[AFR][1000 genomes];0.91[AMR][1000 genomes];0.92[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs34134719	0.85[AMR][1000 genomes];0.87[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs34520011	0.93[ASN][1000 genomes]
rs35194427	0.81[AMR][1000 genomes];0.89[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs4350935	0.89[AMR][1000 genomes];0.93[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs4856889	0.91[AFR][1000 genomes];0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4856890	0.90[AFR][1000 genomes];0.92[ASN][1000 genomes]
rs6768970	0.90[AFR][1000 genomes];0.90[ASN][1000 genomes]
rs6795108	0.81[ASN][1000 genomes]
rs6798796	0.93[AFR][1000 genomes];0.90[ASN][1000 genomes]
rs68005467	0.85[AMR][1000 genomes];0.86[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7618120	0.89[AFR][1000 genomes];0.89[AMR][1000 genomes];0.90[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7642815	0.83[AMR][1000 genomes];0.85[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9824545	0.82[AFR][1000 genomes];0.89[AMR][1000 genomes];0.93[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs9833922	0.90[AFR][1000 genomes];0.90[ASN][1000 genomes]
rs9855740	0.93[AFR][1000 genomes];0.91[ASN][1000 genomes]
rs9857889	0.94[AFR][1000 genomes];0.94[AMR][1000 genomes];0.91[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9871660	0.87[AMR][1000 genomes];0.85[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs9871777	0.94[AFR][1000 genomes];0.91[ASN][1000 genomes]
rs993597	0.91[AMR][1000 genomes];0.93[EUR][1000 genomes];0.94[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv470638	chr3:67367341-67814738	Weak transcription ZNF genes & repeats Enhancers Active TSS Strong transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
2	esv3359258	chr3:67589615-67828274	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
3	nsv1002010	chr3:67785913-68312064	Enhancers Flanking Active TSS Weak transcription Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:12 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:67721400-67800400	Weak transcription	Left Ventricle	heart
2	chr3:67785800-67791600	Enhancers	Primary T helper cells fromperipheralblood	blood
3	chr3:67786000-67791600	Enhancers	Primary T killer naive cells fromperipheralblood	blood
4	chr3:67788000-67802800	Weak transcription	Right Ventricle	heart
5	chr3:67788800-67790800	Enhancers	Primary T cells from cord blood	blood
6	chr3:67788800-67790800	Enhancers	Primary T helper naive cells from peripheral blood	blood
7	chr3:67788800-67792000	Enhancers	Primary T helper cells PMA-I stimulated	--
8	chr3:67788800-67792200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
9	chr3:67789400-67799600	Weak transcription	Aorta	Aorta
10	chr3:67790000-67790600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
11	chr3:67790200-67791400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
12	chr3:67790400-67790600	Enhancers	Primary T killer memory cells from peripheral blood	blood

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