Variant report

Variant	rs62156703
Chromosome Location	chr2:67655877-67655878
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 89 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:84)

rs_ID	r²[population]
rs10496153	0.94[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs1063571	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12185591	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12185702	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12988210	0.82[AMR][1000 genomes]
rs12991090	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs12996359	0.94[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs13000557	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs13004747	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs13004765	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs13009070	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs13015319	0.82[AMR][1000 genomes]
rs13015349	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs13016330	0.82[AMR][1000 genomes]
rs13017696	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs13018894	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs13026513	0.82[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs13030037	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs13030211	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs13034744	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs13035051	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs13035754	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs13036061	0.84[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs1521051	0.94[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs17544516	0.82[AMR][1000 genomes]
rs17544551	0.82[AMR][1000 genomes]
rs17545245	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17545301	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17545329	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17603914	0.82[AMR][1000 genomes]
rs2171176	0.94[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs34103917	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs34274370	0.94[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs34281542	0.94[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs34298852	0.94[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs34418651	0.94[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs34493710	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs34547630	0.82[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs34636997	0.94[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs34737312	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs34920978	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs34962808	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs34997300	0.82[AMR][1000 genomes]
rs35002490	0.94[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs35141978	0.82[AMR][1000 genomes]
rs35144434	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs35340993	0.82[AMR][1000 genomes]
rs35382600	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs35503819	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs35570926	0.82[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs35607813	0.94[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs35610403	0.82[AMR][1000 genomes]
rs35686078	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs35777125	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs36098430	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4428006	0.85[EUR][1000 genomes]
rs62154898	0.82[AMR][1000 genomes]
rs62154948	0.94[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs62154949	0.94[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs62154950	0.94[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs62154951	0.94[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs62154952	0.94[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs62154955	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs62154957	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs62154958	0.84[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs62156688	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs62156689	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62156692	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62156693	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs62156695	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62156696	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs62156698	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs62156699	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62156700	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62156702	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62156754	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62156756	0.94[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs62156757	0.94[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs62156758	0.86[AFR][1000 genomes];0.88[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs62158290	0.82[AMR][1000 genomes]
rs71411986	0.94[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs71411987	0.94[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs71411988	0.94[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs7585807	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1008584	chr2:67168244-67703601	Enhancers Flanking Active TSS Weak transcription Strong transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
2	nsv535775	chr2:67168244-67703601	Strong transcription Enhancers Flanking Active TSS Weak transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
3	nsv534389	chr2:67388428-68225338	Enhancers Active TSS ZNF genes & repeats Weak transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	36 gene(s)	inside rSNPs	diseases
4	nsv834249	chr2:67515471-67691605	Weak transcription Strong transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
5	esv3335541	chr2:67577544-67773907	Enhancers Active TSS Weak transcription Strong transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	9 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	chr2:67639200-67673600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr2:67655800-67656200	Weak transcription	Pancreas	Pancrea

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links