Variant report

Variant	rs6922278
Chromosome Location	chr6:163623169-163623170
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr6:163621041..163623760-chr6:163631210..163632977,2	MCF-7	breast:

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

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

rs_ID	r²[population]
rs1022611	0.91[EUR][1000 genomes]
rs1022612	0.88[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs1122682	0.92[EUR][1000 genomes]
rs13206740	0.87[AMR][1000 genomes]
rs13217757	0.83[AMR][1000 genomes]
rs1540922	0.85[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs1970907	0.87[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs4571546	0.82[EUR][1000 genomes]
rs6455871	0.91[EUR][1000 genomes]
rs6917118	0.92[EUR][1000 genomes]
rs6927470	0.87[EUR][1000 genomes]
rs6935990	0.92[EUR][1000 genomes]
rs6937505	0.92[EUR][1000 genomes]
rs6937679	0.92[EUR][1000 genomes]
rs763599	0.88[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs9456841	0.92[EUR][1000 genomes]
rs9458742	0.92[EUR][1000 genomes]
rs9458743	0.93[EUR][1000 genomes]
rs9458748	0.92[EUR][1000 genomes]
rs9458750	0.89[AMR][1000 genomes];0.98[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs9458752	0.85[AMR][1000 genomes]
rs9458753	0.87[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	nsv932127	chr6:163000261-163950870	Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
2	nsv1026490	chr6:163133433-163705708	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
3	nsv869286	chr6:163146342-163697445	Flanking Active TSS Enhancers Weak transcription Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
4	nsv1022610	chr6:163591786-163814041	Weak transcription Enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Strong transcription Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
5	esv275472	chr6:163619906-163623619	Weak transcription Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:163608000-163632800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr6:163616400-163628800	Weak transcription	Brain Cingulate Gyrus	brain
3	chr6:163617800-163623800	Weak transcription	Brain Anterior Caudate	brain
4	chr6:163620200-163623400	Weak transcription	Fetal Heart	heart
5	chr6:163620800-163623600	Weak transcription	Brain Hippocampus Middle	brain
6	chr6:163622800-163630200	Weak transcription	Right Ventricle	heart
7	chr6:163623000-163623200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin

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