Variant report

Variant	rs41270048
Chromosome Location	chr6:35085821-35085822
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 22 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs12110520	1.00[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs12110664	0.81[EUR][1000 genomes]
rs12111424	1.00[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs2004	1.00[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs2894400	0.81[EUR][1000 genomes]
rs35455943	1.00[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs41270046	1.00[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs57976333	1.00[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs58850273	1.00[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs60113507	1.00[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs73403834	1.00[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs73403837	1.00[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs73403843	1.00[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs73403887	1.00[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs73405709	1.00[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs73405725	1.00[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs73405759	0.81[EUR][1000 genomes]
rs73405768	0.81[EUR][1000 genomes]
rs73405774	0.81[EUR][1000 genomes]
rs73405795	0.81[EUR][1000 genomes]
rs73405799	0.81[EUR][1000 genomes]
rs820102	1.00[AMR][1000 genomes];0.81[EUR][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:35085600-35086800	Bivalent Enhancer	HepG2	liver

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Input of quick search could be:

dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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