Variant report

Variant	rs6536923
Chromosome Location	chr4:166506917-166506918
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 8 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:7)

rs_ID	r²[population]
rs1320223	0.92[AMR][1000 genomes]
rs1914841	0.92[AMR][1000 genomes]
rs1914843	0.92[AMR][1000 genomes]
rs4091535	0.92[AMR][1000 genomes]
rs4691207	0.92[AMR][1000 genomes]
rs6855009	0.85[AMR][1000 genomes]
rs7692810	0.92[AMR][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv830141	chr4:166502908-166689626	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:166502000-166509000	Weak transcription	Colon Smooth Muscle	Colon
2	chr4:166502800-166508600	Weak transcription	Fetal Heart	heart
3	chr4:166503000-166523800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr4:166504400-166507200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
5	chr4:166504800-166509600	Weak transcription	HUVEC	blood vessel

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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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