Variant report

Variant	rs1462795
Chromosome Location	chr3:110692754-110692755
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 116 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:110)

rs_ID	r²[population]
rs1075303	0.95[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11717706	0.81[AFR][1000 genomes]
rs11919892	0.84[AFR][1000 genomes]
rs11927478	0.84[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11929280	0.85[CEU][hapmap]
rs13060876	0.82[AFR][1000 genomes]
rs13061640	0.82[AFR][1000 genomes]
rs13072462	0.81[AFR][1000 genomes]
rs1350980	0.91[AFR][1000 genomes];0.89[AMR][1000 genomes];0.92[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs1381828	0.86[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1381836	0.85[CEU][hapmap]
rs1382075	0.82[AFR][1000 genomes]
rs1462789	0.95[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1462790	1.00[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1462793	0.91[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1462801	0.85[EUR][1000 genomes]
rs1462807	0.91[ASN][1000 genomes]
rs1477843	1.00[CEU][hapmap];0.94[CHB][hapmap]
rs1477846	1.00[CEU][hapmap]
rs1477847	1.00[CEU][hapmap];0.95[CHB][hapmap];0.81[AFR][1000 genomes]
rs1477848	1.00[CEU][hapmap]
rs1477850	0.85[CEU][hapmap]
rs1477851	0.86[CEU][hapmap]
rs1477854	0.84[AFR][1000 genomes]
rs1477855	0.84[AFR][1000 genomes]
rs1580288	0.98[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1585594	0.94[AFR][1000 genomes];0.94[AMR][1000 genomes];0.92[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1585595	0.83[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1599663	0.97[AFR][1000 genomes];0.94[AMR][1000 genomes];0.92[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1599664	0.97[AFR][1000 genomes];0.94[AMR][1000 genomes];0.92[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1600059	0.84[AFR][1000 genomes]
rs16857350	0.85[CEU][hapmap]
rs16857483	0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1824666	0.97[AFR][1000 genomes];0.94[AMR][1000 genomes];0.92[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1871026	0.81[AFR][1000 genomes]
rs1903755	1.00[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1903759	0.82[AFR][1000 genomes];0.89[AMR][1000 genomes];0.91[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs1993802	0.85[EUR][1000 genomes]
rs1993803	0.81[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs2002969	0.86[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2100875	0.94[AFR][1000 genomes];0.91[AMR][1000 genomes];0.92[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2126710	0.82[AFR][1000 genomes]
rs2126713	1.00[CEU][hapmap];0.94[CHB][hapmap];0.81[AFR][1000 genomes]
rs2169643	0.85[CEU][hapmap]
rs2399367	0.89[ASN][1000 genomes]
rs2399368	0.89[ASN][1000 genomes]
rs2399370	0.96[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2399371	0.82[EUR][1000 genomes]
rs2399373	1.00[CEU][hapmap];0.89[CHB][hapmap];0.81[AFR][1000 genomes]
rs2399375	1.00[CEU][hapmap]
rs2399378	0.95[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2895376	0.99[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs35665971	0.81[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4102676	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4234401	0.93[AFR][1000 genomes];0.89[AMR][1000 genomes];0.92[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs4682028	0.97[AFR][1000 genomes];0.91[AMR][1000 genomes];0.92[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs4682215	0.89[ASN][1000 genomes]
rs4682229	1.00[CEU][hapmap];0.94[CHB][hapmap]
rs4682230	1.00[CEU][hapmap];0.94[CHB][hapmap];0.81[AFR][1000 genomes]
rs4682231	1.00[CEU][hapmap];0.95[CHB][hapmap];0.81[AFR][1000 genomes]
rs4682234	1.00[CEU][hapmap];0.94[CHB][hapmap]
rs4682238	1.00[CEU][hapmap]
rs5000277	0.93[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6437940	0.95[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6437948	1.00[CEU][hapmap];0.94[CHB][hapmap]
rs6437953	1.00[CEU][hapmap]
rs66513024	0.83[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs67056469	0.83[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6763050	0.85[CEU][hapmap]
rs6765948	0.85[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs6781480	0.82[AFR][1000 genomes]
rs67832786	0.91[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6787921	0.90[ASN][1000 genomes]
rs6790828	0.81[AFR][1000 genomes]
rs6794645	1.00[CEU][hapmap]
rs6805399	0.84[AFR][1000 genomes];0.86[AMR][1000 genomes];0.86[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6808847	0.86[AFR][1000 genomes];0.89[AMR][1000 genomes];0.90[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs723023	0.98[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs723025	0.83[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7430600	1.00[CEU][hapmap]
rs7433877	0.85[CEU][hapmap]
rs7610760	1.00[CEU][hapmap]
rs7612572	0.81[AFR][1000 genomes]
rs7612667	1.00[CEU][hapmap];0.94[CHB][hapmap];0.81[AFR][1000 genomes]
rs7622983	0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7623003	0.85[EUR][1000 genomes]
rs7623064	0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7623103	0.81[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7623880	1.00[CEU][hapmap]
rs7632375	0.82[AFR][1000 genomes]
rs7632388	0.82[AFR][1000 genomes]
rs7637068	0.83[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7644948	0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7648752	0.82[CEU][hapmap]
rs873132	0.85[CEU][hapmap]
rs9288918	0.85[CEU][hapmap]
rs969940	0.85[CEU][hapmap]
rs9817950	0.98[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs9821335	1.00[CEU][hapmap];0.94[CHB][hapmap]
rs9826064	1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9828899	1.00[CEU][hapmap];0.94[CHB][hapmap];0.81[AFR][1000 genomes]
rs9837377	0.84[AFR][1000 genomes]
rs9839299	0.97[AFR][1000 genomes];0.89[AMR][1000 genomes];0.92[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs9839674	1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9847598	0.84[AFR][1000 genomes]
rs9866028	1.00[CEU][hapmap];0.94[CHB][hapmap]
rs9876350	1.00[CEU][hapmap];0.95[CHB][hapmap];0.81[AFR][1000 genomes]
rs9876543	0.82[AFR][1000 genomes];0.89[AMR][1000 genomes];0.91[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs9877855	0.84[AFR][1000 genomes]
rs9882945	0.85[CEU][hapmap]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1003106	chr3:110264476-111105943	Weak transcription Enhancers Strong transcription Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
2	nsv1014199	chr3:110293896-110754155	Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Strong transcription Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
3	nsv829674	chr3:110616256-110771049	Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Active TSS Flanking Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
4	nsv460821	chr3:110637471-111501097	Enhancers Active TSS Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Weak transcription Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
5	nsv591275	chr3:110637471-111501097	Strong transcription Enhancers Weak transcription ZNF genes & repeats Active TSS Bivalent/Poised TSS Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
6	esv1850918	chr3:110685181-110889974	Bivalent Enhancer Weak transcription Enhancers Flanking Bivalent TSS/Enh Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:110683800-110703000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr3:110692600-110693000	Enhancers	Dnd41	blood
3	chr3:110692600-110693200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin

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