Variant report

Variant	rs162268
Chromosome Location	chr3:78962148-78962149
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 68 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:61)

rs_ID	r²[population]
rs13075210	0.91[CHB][hapmap];0.80[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs162262	0.86[CHB][hapmap]
rs162263	0.91[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.86[JPT][hapmap];0.85[MEX][hapmap];0.87[TSI][hapmap];0.81[AMR][1000 genomes];0.90[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs162264	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs162265	0.91[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.90[AFR][1000 genomes];0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs162266	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs162267	0.83[AMR][1000 genomes];0.92[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs162423	0.80[CHB][hapmap]
rs162425	0.90[CEU][hapmap];0.83[CHB][hapmap];0.81[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs162426	0.81[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs162427	0.81[CHB][hapmap];0.83[EUR][1000 genomes]
rs162428	0.93[CHB][hapmap];0.82[EUR][1000 genomes]
rs162429	0.93[CHB][hapmap];0.80[CHD][hapmap];0.86[MEX][hapmap];0.88[TSI][hapmap];0.83[EUR][1000 genomes]
rs17313732	0.86[CHB][hapmap]
rs186648	0.93[EUR][1000 genomes]
rs186688	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[YRI][hapmap];0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs328045	0.91[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.86[JPT][hapmap];0.85[MEX][hapmap];0.87[TSI][hapmap];0.81[AMR][1000 genomes];0.90[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs328047	1.00[CEU][hapmap];1.00[CHB][hapmap];0.80[CHD][hapmap];0.93[MEX][hapmap];0.86[TSI][hapmap];0.90[EUR][1000 genomes]
rs329805	0.93[CHB][hapmap];0.81[EUR][1000 genomes]
rs329813	0.86[CHB][hapmap]
rs329814	0.88[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.93[JPT][hapmap];0.93[TSI][hapmap];0.87[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs329815	0.92[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs329816	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.82[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs329817	0.92[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs329818	0.88[EUR][1000 genomes]
rs329819	0.88[CEU][hapmap];0.93[CHB][hapmap];0.80[CHD][hapmap];0.95[TSI][hapmap];0.90[EUR][1000 genomes]
rs329820	0.91[EUR][1000 genomes]
rs329821	0.88[EUR][1000 genomes]
rs329822	0.87[CEU][hapmap];1.00[CHB][hapmap];0.82[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs329824	0.81[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs329825	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap];0.95[AFR][1000 genomes];0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs331149	0.91[CHD][hapmap];0.82[TSI][hapmap]
rs331158	0.86[CHB][hapmap]
rs331181	0.90[EUR][1000 genomes]
rs331182	0.82[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs331183	0.82[AMR][1000 genomes];0.85[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs331184	0.91[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs331188	0.82[EUR][1000 genomes]
rs331189	0.87[EUR][1000 genomes]
rs331190	0.85[EUR][1000 genomes]
rs331199	0.96[CEU][hapmap];1.00[CHB][hapmap];0.83[CHD][hapmap];0.95[TSI][hapmap];0.95[EUR][1000 genomes]
rs369346	1.00[CEU][hapmap];1.00[CHB][hapmap];0.88[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs379346	1.00[CEU][hapmap];1.00[CHB][hapmap];0.88[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs387900	1.00[CEU][hapmap];1.00[CHB][hapmap];0.92[EUR][1000 genomes]
rs388421	0.88[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs409361	0.87[EUR][1000 genomes]
rs420481	0.98[AFR][1000 genomes];0.97[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs425121	0.94[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs432141	0.84[ASN][1000 genomes]
rs434929	0.93[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs453354	0.81[AMR][1000 genomes];0.90[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs4681013	0.84[CHB][hapmap]
rs479956	0.91[CEU][hapmap];1.00[CHB][hapmap];0.86[JPT][hapmap];0.86[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs484531	0.88[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs498805	0.91[CEU][hapmap];1.00[CHB][hapmap];0.95[CHD][hapmap];0.86[JPT][hapmap];0.93[MEX][hapmap];0.86[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs512135	0.86[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs6548601	0.96[CEU][hapmap];1.00[CHB][hapmap];0.81[EUR][1000 genomes]
rs6772919	0.96[CEU][hapmap];1.00[CHB][hapmap];0.81[EUR][1000 genomes]
rs6800782	0.91[CEU][hapmap];1.00[CHB][hapmap];0.85[JPT][hapmap];0.88[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7617538	0.87[CEU][hapmap];1.00[CHB][hapmap];0.84[ASN][1000 genomes]
rs7619765	0.83[AFR][1000 genomes];0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1010804	chr3:78739648-79087470	Enhancers Flanking Active TSS Active TSS Weak transcription Strong transcription Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
2	nsv533681	chr3:78750924-79017336	Weak transcription Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
3	nsv834744	chr3:78911545-79076470	Flanking Active TSS Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
4	nsv877020	chr3:78913203-78975982	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
5	nsv470672	chr3:78913203-78985805	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
6	nsv590734	chr3:78915205-78985805	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
7	nsv590735	chr3:78922852-78977507	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:78956400-78962200	Weak transcription	HUES6 Cell Line	embryonic stem cell
2	chr3:78956800-78962800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
3	chr3:78958000-78963000	Weak transcription	HepG2	liver
4	chr3:78959600-78987200	Weak transcription	Fetal Lung	lung
5	chr3:78961400-78962800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
6	chr3:78961600-78963200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
7	chr3:78962000-78963000	Weak transcription	A549	lung
8	chr3:78962000-78967400	Weak transcription	Pancreatic Islets	Pancreatic Islet

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links