Variant report

Variant	rs11752633
Chromosome Location	chr6:163618770-163618771
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 26 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:21)

rs_ID	r²[population]
rs1022611	0.91[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs13197837	0.91[EUR][1000 genomes]
rs13206290	0.91[EUR][1000 genomes]
rs13206740	0.91[EUR][1000 genomes]
rs13217757	0.93[EUR][1000 genomes]
rs13219179	0.91[EUR][1000 genomes]
rs4571546	0.84[AMR][1000 genomes]
rs4708981	0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs5005309	0.86[EUR][1000 genomes]
rs6455871	0.95[AMR][1000 genomes];0.85[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6916143	0.98[AMR][1000 genomes];0.95[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs6917118	0.94[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs6927470	0.92[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs6935990	0.95[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs6937505	0.95[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs6937679	0.95[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs9456841	0.92[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs9458742	0.94[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs9458743	0.94[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs9458752	0.92[EUR][1000 genomes]
rs9458753	0.92[EUR][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	esv2762628	chr6:163572148-163620903	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
5	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

No data

Chromatin state (count:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:163602600-163622600	Weak transcription	Right Ventricle	heart
2	chr6:163608000-163632800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr6:163614000-163621200	Weak transcription	Skeletal Muscle Male	skeletal muscle
4	chr6:163614200-163618800	Weak transcription	Fetal Heart	heart
5	chr6:163616400-163628800	Weak transcription	Brain Cingulate Gyrus	brain
6	chr6:163617800-163620400	Weak transcription	Brain Substantia Nigra	brain
7	chr6:163617800-163623800	Weak transcription	Brain Anterior Caudate	brain
8	chr6:163618000-163619400	Weak transcription	Brain Inferior Temporal Lobe	brain
9	chr6:163618000-163620400	Weak transcription	Brain Hippocampus Middle	brain

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