Variant report

Variant	rs2921756
Chromosome Location	chr8:117915471-117915472
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 60 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:58)

rs_ID	r²[population]
rs10282816	0.91[ASN][1000 genomes]
rs12543129	0.91[ASN][1000 genomes]
rs12548885	0.90[ASN][1000 genomes]
rs12548895	0.91[ASN][1000 genomes]
rs1348797	0.97[ASN][1000 genomes]
rs14795	1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[ASN][1000 genomes]
rs16888870	0.91[ASN][1000 genomes]
rs2241981	1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[ASN][1000 genomes]
rs2241982	1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[ASN][1000 genomes]
rs2921754	0.92[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs2921757	0.91[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs2921758	1.00[ASN][1000 genomes]
rs2921770	0.91[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs2921771	0.97[ASN][1000 genomes]
rs2921772	0.91[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs2921773	0.97[ASN][1000 genomes]
rs2921774	0.91[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs2921775	1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs2921776	0.97[ASN][1000 genomes]
rs2921777	0.97[ASN][1000 genomes]
rs2921778	0.97[ASN][1000 genomes]
rs2921779	0.97[ASN][1000 genomes]
rs2921780	0.97[ASN][1000 genomes]
rs2921781	0.97[ASN][1000 genomes]
rs2921782	0.97[ASN][1000 genomes]
rs2921783	0.97[ASN][1000 genomes]
rs2921784	1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs2921785	1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs2921786	0.97[ASN][1000 genomes]
rs2921787	1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs2921788	1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs2921789	1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[ASN][1000 genomes]
rs2921790	1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[ASN][1000 genomes]
rs2921791	1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[ASN][1000 genomes]
rs3020109	1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[ASN][1000 genomes]
rs3020111	1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs3020118	0.97[ASN][1000 genomes]
rs3020124	0.97[ASN][1000 genomes]
rs3020125	1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs3020126	0.97[ASN][1000 genomes]
rs3020128	0.97[ASN][1000 genomes]
rs3020130	0.97[ASN][1000 genomes]
rs3020131	0.97[ASN][1000 genomes]
rs3020133	1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[ASN][1000 genomes]
rs3020134	0.97[ASN][1000 genomes]
rs3020135	0.94[ASN][1000 genomes]
rs3020136	0.91[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs3020138	0.97[ASN][1000 genomes]
rs3020139	0.97[ASN][1000 genomes]
rs3020140	0.91[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs3020142	0.97[ASN][1000 genomes]
rs3020174	0.93[JPT][hapmap]
rs3020181	1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs35189908	0.81[ASN][1000 genomes]
rs56095633	0.91[ASN][1000 genomes]
rs57202151	0.91[ASN][1000 genomes]
rs6996153	1.00[CHB][hapmap];0.92[JPT][hapmap]
rs73308296	0.88[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv530386	chr8:117509968-118391406	Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
2	nsv831434	chr8:117784467-117977825	Flanking Active TSS Genic enhancers Weak transcription Enhancers Active TSS Bivalent/Poised TSS Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	17 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:117912800-117915600	Enhancers	Hela-S3	cervix
2	chr8:117913200-117915800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
3	chr8:117913200-117915800	Enhancers	HMEC	breast
4	chr8:117914000-117915600	Flanking Active TSS	Dnd41	blood
5	chr8:117914000-117915800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
6	chr8:117915400-117916400	Enhancers	HSMMtube	muscle

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