Variant report

Variant	rs294470
Chromosome Location	chr3:142905461-142905462
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr3:142904057..142907019-chr3:142910125..142912001,3	K562	blood:
2	chr3:142901683..142905677-chr3:142909688..142913196,5	K562	blood:

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

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

rs_ID	r²[population]
rs10935485	0.88[ASN][1000 genomes]
rs11715203	0.93[ASN][1000 genomes]
rs1667712	0.90[ASN][1000 genomes]
rs169808	0.92[ASN][1000 genomes]
rs186077	0.93[ASN][1000 genomes]
rs2165519	0.90[ASN][1000 genomes]
rs2165520	0.93[ASN][1000 genomes]
rs2583458	0.90[ASN][1000 genomes]
rs2596616	0.91[ASN][1000 genomes]
rs294465	0.93[ASN][1000 genomes]
rs294469	0.92[ASN][1000 genomes]
rs294471	0.93[ASN][1000 genomes]
rs294472	0.92[ASN][1000 genomes]
rs294473	0.92[ASN][1000 genomes]
rs4371486	0.89[CHB][hapmap];0.93[CHD][hapmap];0.94[JPT][hapmap];0.92[ASN][1000 genomes]
rs4683461	0.94[CHB][hapmap];0.96[CHD][hapmap];0.89[JPT][hapmap];0.88[ASN][1000 genomes]
rs4839588	0.93[ASN][1000 genomes]
rs4839591	0.93[ASN][1000 genomes]
rs4839616	0.92[ASN][1000 genomes]
rs4839617	0.92[ASN][1000 genomes]
rs4839618	0.92[ASN][1000 genomes]
rs4839619	0.93[ASN][1000 genomes]
rs4839621	0.92[ASN][1000 genomes]
rs4839625	0.88[ASN][1000 genomes]
rs4839629	0.93[ASN][1000 genomes]
rs4839656	0.93[ASN][1000 genomes]
rs54520	0.89[CHB][hapmap];0.94[JPT][hapmap];0.93[ASN][1000 genomes]
rs6414352	0.92[ASN][1000 genomes]
rs6440149	0.92[ASN][1000 genomes]
rs6440150	0.92[ASN][1000 genomes]
rs6440151	0.92[ASN][1000 genomes]
rs6440152	0.92[ASN][1000 genomes]
rs6440153	0.93[ASN][1000 genomes]
rs6765181	0.93[ASN][1000 genomes]
rs6767762	0.88[ASN][1000 genomes]
rs6776634	0.93[ASN][1000 genomes]
rs6777882	0.93[ASN][1000 genomes]
rs6778330	0.93[ASN][1000 genomes]
rs6781821	0.92[ASN][1000 genomes]
rs6781909	0.92[ASN][1000 genomes]
rs6785002	0.93[ASN][1000 genomes]
rs6785085	0.91[ASN][1000 genomes]
rs6786129	0.92[ASN][1000 genomes]
rs6788806	0.88[ASN][1000 genomes]
rs6795908	0.93[ASN][1000 genomes]
rs6796353	0.93[ASN][1000 genomes]
rs6803862	0.92[ASN][1000 genomes]
rs7611317	0.92[ASN][1000 genomes]
rs7622977	0.90[ASN][1000 genomes]
rs7632649	0.92[ASN][1000 genomes]
rs834906	0.93[ASN][1000 genomes]
rs834907	0.92[ASN][1000 genomes]
rs834908	0.92[ASN][1000 genomes]
rs834909	0.92[ASN][1000 genomes]
rs834910	0.92[ASN][1000 genomes]
rs9289656	0.93[ASN][1000 genomes]
rs9809153	0.92[ASN][1000 genomes]
rs9821086	0.88[CHB][hapmap];0.94[JPT][hapmap]
rs9847552	0.89[ASN][1000 genomes]
rs990738	0.93[ASN][1000 genomes]
rs991419	0.93[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	esv2757893	chr3:142720230-142962932	Enhancers Active TSS Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
2	esv2759183	chr3:142720230-142964373	Strong transcription Weak transcription Enhancers Bivalent Enhancer Active TSS Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
3	nsv949288	chr3:142793323-143585882	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Strong transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	24 gene(s)	inside rSNPs	diseases
4	nsv508250	chr3:142842454-142943722	Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
5	esv34280	chr3:142887460-142962075	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Strong transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
6	nsv818171	chr3:142894411-142960273	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
7	nsv1009573	chr3:142896048-142959777	Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Active TSS ZNF genes & repeats Strong transcription Genic enhancers	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:142893200-142909200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
2	chr3:142902400-142908600	Weak transcription	Primary T cells from cord blood	blood
3	chr3:142902600-142909200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
4	chr3:142902600-142909200	Weak transcription	Primary T helper cells PMA-I stimulated	--
5	chr3:142903000-142906800	Enhancers	K562	blood
6	chr3:142903200-142908000	Weak transcription	Fetal Thymus	thymus
7	chr3:142904800-142906600	Enhancers	Dnd41	blood

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