Variant report

Variant	rs526635
Chromosome Location	chr6:49265452-49265453
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 71 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:69)

rs_ID	r²[population]
rs16878901	0.80[AFR][1000 genomes]
rs16878906	0.80[AFR][1000 genomes]
rs472168	0.92[AFR][1000 genomes]
rs473800	0.84[AFR][1000 genomes]
rs476131	0.80[YRI][hapmap]
rs476657	0.90[AFR][1000 genomes]
rs477051	1.00[YRI][hapmap]
rs478469	0.80[AFR][1000 genomes]
rs478991	0.83[YRI][hapmap]
rs480061	0.80[AFR][1000 genomes]
rs482046	0.88[AFR][1000 genomes]
rs483257	0.80[AFR][1000 genomes]
rs484563	0.90[AFR][1000 genomes]
rs484612	0.90[AFR][1000 genomes]
rs485743	0.80[AFR][1000 genomes]
rs486435	0.90[AFR][1000 genomes]
rs487363	0.90[AFR][1000 genomes]
rs488497	0.92[AFR][1000 genomes]
rs489459	0.82[AFR][1000 genomes]
rs491967	0.80[AFR][1000 genomes]
rs493691	0.86[AFR][1000 genomes]
rs494529	0.80[AFR][1000 genomes]
rs495233	0.92[AFR][1000 genomes]
rs496080	0.92[AFR][1000 genomes]
rs497390	0.92[AFR][1000 genomes]
rs498048	0.92[AFR][1000 genomes]
rs498264	0.90[AFR][1000 genomes]
rs498367	0.90[AFR][1000 genomes]
rs498400	0.82[AFR][1000 genomes]
rs501968	0.92[AFR][1000 genomes]
rs502868	0.90[AFR][1000 genomes]
rs505273	0.90[AFR][1000 genomes]
rs510455	0.83[YRI][hapmap]
rs513031	0.83[YRI][hapmap]
rs514138	0.83[YRI][hapmap]
rs516988	0.86[AFR][1000 genomes]
rs517774	0.92[AFR][1000 genomes]
rs520470	0.83[YRI][hapmap]
rs522061	0.92[AFR][1000 genomes]
rs523897	0.90[AFR][1000 genomes]
rs524822	0.92[AFR][1000 genomes]
rs525892	0.92[AFR][1000 genomes]
rs529393	0.90[AFR][1000 genomes]
rs539427	0.83[YRI][hapmap]
rs539659	1.00[YRI][hapmap]
rs539754	0.83[YRI][hapmap]
rs544263	0.83[YRI][hapmap]
rs546248	0.86[AFR][1000 genomes]
rs547609	0.88[AFR][1000 genomes]
rs550485	0.80[AFR][1000 genomes]
rs550645	0.92[AFR][1000 genomes]
rs552336	0.88[AFR][1000 genomes]
rs552383	0.80[AFR][1000 genomes]
rs553567	0.92[AFR][1000 genomes]
rs554083	0.92[AFR][1000 genomes]
rs558669	0.90[AFR][1000 genomes]
rs559706	0.88[AFR][1000 genomes]
rs560700	0.90[AFR][1000 genomes]
rs561215	0.80[AFR][1000 genomes]
rs563111	0.83[YRI][hapmap]
rs563878	0.92[AFR][1000 genomes]
rs565793	0.88[AFR][1000 genomes]
rs567539	0.88[AFR][1000 genomes]
rs568143	0.83[YRI][hapmap]
rs571802	0.80[AFR][1000 genomes]
rs574868	0.80[AFR][1000 genomes]
rs575461	0.83[YRI][hapmap]
rs578848	0.92[AFR][1000 genomes]
rs579011	0.92[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv949690	chr6:48595821-49289855	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	esv2755862	chr6:49081541-49298041	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Strong transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:49263600-49266400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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