Variant report

Variant	rs73241724
Chromosome Location	chr6:164105628-164105629
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr6:164104118..164105951-chr6:164112390..164114240,2	K562	blood:

Extended variants
information (count: 27 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:22)

rs_ID	r²[population]
rs56984848	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs57235208	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs57308664	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs57456277	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs57524107	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs57770616	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs58214854	1.00[AFR][1000 genomes]
rs59039271	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs60755658	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73236460	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73236470	1.00[AMR][1000 genomes]
rs73241725	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73241734	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73241736	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73241742	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73241743	0.91[AFR][1000 genomes]
rs73241745	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73241748	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73241750	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73241752	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73241755	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73241765	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1018860	chr6:163939347-164532579	Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Active TSS Genic enhancers Strong transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
2	nsv538526	chr6:163939347-164532579	Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
3	esv2758092	chr6:163992064-164161903	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Strong transcription Genic enhancers ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
4	esv2759490	chr6:163992064-164161903	Strong transcription Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Genic enhancers ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
5	nsv1019107	chr6:164056423-164144164	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	8 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	chr6:164102600-164110200	Weak transcription	Fetal Heart	heart
2	chr6:164105600-164106000	Enhancers	GM12878-XiMat	blood
3	chr6:164105600-164107000	Enhancers	Primary B cells from peripheral blood	blood

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