Variant report

Variant	rs6904708
Chromosome Location	chr6:147421172-147421173
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr6:147417432..147420114-chr6:147420154..147422310,2	K562	blood:
2	chr6:147417345..147419062-chr6:147421099..147422662,2	K562	blood:
3	chr6:147420322..147423479-chr6:147424445..147428438,5	K562	blood:
4	chr6:147419431..147422088-chr6:147424854..147426764,2	MCF-7	breast:
5	chr6:147420000..147421600-chr6:147444950..147446900,2	K562	blood:
6	chr6:147420588..147422113-chr6:147425783..147427483,2	K562	blood:

Extended variants
information (count: 57 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:54)

rs_ID	r²[population]
rs1113883	0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11967383	0.89[ASN][1000 genomes]
rs11969474	0.89[ASN][1000 genomes]
rs12111514	0.89[ASN][1000 genomes]
rs12661078	0.89[ASN][1000 genomes]
rs12661753	0.81[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12664201	1.00[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12664682	0.93[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12664716	0.81[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1529012	1.00[CEU][hapmap];0.82[CHB][hapmap];0.86[JPT][hapmap];0.91[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs17076589	0.83[ASN][1000 genomes]
rs17076610	1.00[CHB][hapmap];0.89[ASN][1000 genomes]
rs58134586	0.96[ASN][1000 genomes]
rs58922329	1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs59578647	0.92[ASN][1000 genomes]
rs61443164	0.88[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6902096	1.00[AFR][1000 genomes]
rs6907758	0.89[ASN][1000 genomes]
rs6909582	1.00[CHB][hapmap];0.86[JPT][hapmap];0.96[ASN][1000 genomes]
rs6913549	0.96[ASN][1000 genomes]
rs6913672	0.89[ASN][1000 genomes]
rs6915603	0.82[EUR][1000 genomes]
rs6916236	0.89[ASN][1000 genomes]
rs6917323	0.91[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs6920520	0.96[ASN][1000 genomes]
rs6924581	0.89[ASN][1000 genomes]
rs6924985	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6925187	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6925324	0.90[AFR][1000 genomes]
rs6925633	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6929579	0.96[ASN][1000 genomes]
rs73588114	0.89[ASN][1000 genomes]
rs73588127	0.92[ASN][1000 genomes]
rs73588137	0.96[ASN][1000 genomes]
rs73588149	0.96[ASN][1000 genomes]
rs73590029	0.92[ASN][1000 genomes]
rs7764355	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7773216	0.89[ASN][1000 genomes]
rs9322091	1.00[JPT][hapmap]
rs9322092	0.82[EUR][1000 genomes]
rs9322093	1.00[CEU][hapmap];1.00[JPT][hapmap]
rs9485137	0.83[ASN][1000 genomes]
rs9485142	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9485144	0.97[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs9485149	1.00[JPT][hapmap]
rs9497695	1.00[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9497696	1.00[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9497697	0.92[AFR][1000 genomes]
rs9497707	0.82[CHB][hapmap];1.00[JPT][hapmap];0.91[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs9497709	1.00[CEU][hapmap]
rs9497715	1.00[CEU][hapmap];1.00[JPT][hapmap]
rs9791310	0.96[ASN][1000 genomes]
rs9791311	0.96[ASN][1000 genomes]
rs9885771	0.98[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1019245	chr6:147350834-147609776	Weak transcription Enhancers Active TSS Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	25 gene(s)	inside rSNPs	diseases
2	nsv538467	chr6:147350834-147609776	Weak transcription Flanking Active TSS Genic enhancers Enhancers Active TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	25 gene(s)	inside rSNPs	diseases
3	nsv886751	chr6:147354092-147490398	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:13 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:147421000-147421400	Enhancers	HUVEC	blood vessel
2	chr6:147421000-147421800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
3	chr6:147421000-147421800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
4	chr6:147421000-147421800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
5	chr6:147421000-147421800	Enhancers	HSMM	muscle
6	chr6:147421000-147421800	Enhancers	HSMMtube	muscle
7	chr6:147421000-147421800	Enhancers	NHLF	lung
8	chr6:147421000-147422000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
9	chr6:147421000-147422000	Enhancers	Muscle Satellite Cultured Cells	--
10	chr6:147421000-147422000	Enhancers	K562	blood
11	chr6:147421000-147422000	Enhancers	NH-A	brain
12	chr6:147421000-147422000	Enhancers	NHDF-Ad	bronchial
13	chr6:147421000-147422000	Enhancers	Osteobl	bone

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