Variant report

Variant	rs768686
Chromosome Location	chr3:110637471-110637472
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 55 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:49)

rs_ID	r²[population]
rs10511291	0.81[ASN][1000 genomes]
rs10755069	1.00[EUR][1000 genomes]
rs12493974	0.96[ASN][1000 genomes]
rs1350930	1.00[EUR][1000 genomes]
rs1350979	0.83[ASN][1000 genomes]
rs1381830	0.83[ASN][1000 genomes]
rs1381833	0.83[ASN][1000 genomes]
rs1381834	0.85[ASN][1000 genomes]
rs1381835	0.85[ASN][1000 genomes]
rs1381836	0.85[CEU][hapmap];1.00[CHB][hapmap];0.94[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.85[ASN][1000 genomes]
rs1462299	0.83[ASN][1000 genomes]
rs1462308	0.90[EUR][1000 genomes]
rs1462326	0.97[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs1462798	0.96[ASN][1000 genomes]
rs1462802	0.83[ASN][1000 genomes]
rs1477846	1.00[CHB][hapmap];0.88[CHD][hapmap]
rs1477848	1.00[CHB][hapmap];0.88[CHD][hapmap]
rs1542513	1.00[EUR][1000 genomes]
rs16857350	0.85[CEU][hapmap];1.00[CHB][hapmap];0.94[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.85[ASN][1000 genomes]
rs16857373	0.96[ASN][1000 genomes]
rs16857536	0.81[ASN][1000 genomes]
rs1870926	0.83[ASN][1000 genomes]
rs2045784	0.85[ASN][1000 genomes]
rs2169497	1.00[EUR][1000 genomes]
rs2169565	0.83[ASN][1000 genomes]
rs2219706	0.96[ASN][1000 genomes]
rs2399364	0.85[ASN][1000 genomes]
rs2399369	0.85[ASN][1000 genomes]
rs4682027	0.83[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs60037602	0.83[ASN][1000 genomes]
rs6437934	1.00[ASN][1000 genomes]
rs6763050	0.85[CEU][hapmap];1.00[CHB][hapmap];0.94[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.85[ASN][1000 genomes]
rs6805467	1.00[ASN][1000 genomes]
rs72934030	0.89[ASN][1000 genomes]
rs72934034	0.89[ASN][1000 genomes]
rs72934100	0.81[ASN][1000 genomes]
rs72935934	0.81[ASN][1000 genomes]
rs72948795	0.83[ASN][1000 genomes]
rs72948800	0.83[ASN][1000 genomes]
rs7433877	0.85[CEU][hapmap];1.00[CHB][hapmap];0.88[CHD][hapmap];0.83[GIH][hapmap]
rs7629008	0.83[ASN][1000 genomes]
rs7648752	0.82[CEU][hapmap];1.00[CHB][hapmap]
rs7650516	0.83[ASN][1000 genomes]
rs768685	0.82[ASN][1000 genomes]
rs873132	0.85[CEU][hapmap];1.00[CHB][hapmap];0.94[CHD][hapmap];0.83[GIH][hapmap]
rs9288918	0.85[CEU][hapmap];1.00[CHB][hapmap];0.88[CHD][hapmap];0.83[GIH][hapmap]
rs936512	0.83[ASN][1000 genomes]
rs969940	0.85[CEU][hapmap];1.00[CHB][hapmap];0.94[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.85[ASN][1000 genomes]
rs9839231	0.87[ASN][1000 genomes]

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	esv2762345	chr3:110614389-110668843	Enhancers ZNF genes & repeats Weak transcription Strong transcription Flanking Active TSS Genic enhancers Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
4	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
5	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
6	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

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:110620200-110653800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr3:110636400-110638800	Enhancers	iPS-18 Cell Line	embryonic stem cell
3	chr3:110636800-110638000	Enhancers	Fetal Lung	lung
4	chr3:110637200-110637800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
5	chr3:110637200-110638800	Enhancers	HUES64 Cell Line	embryonic stem cell
6	chr3:110637200-110639600	Weak transcription	H1 Cell Line	embryonic stem cell
7	chr3:110637200-110646000	Weak transcription	H9 Cell Line	embryonic stem cell
8	chr3:110637400-110638600	Enhancers	HUES48 Cell Line	embryonic stem cell
9	chr3:110637400-110638600	Enhancers	iPS-20b Cell Line	embryonic stem cell

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