Variant report

Variant	rs72673569
Chromosome Location	chr1:56461586-56461587
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 11 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:9)

rs_ID	r²[population]
rs12125033	0.93[ASN][1000 genomes]
rs12136504	0.97[ASN][1000 genomes]
rs55695312	0.97[ASN][1000 genomes]
rs56332616	0.93[ASN][1000 genomes]
rs6588598	0.97[ASN][1000 genomes]
rs6588599	0.97[ASN][1000 genomes]
rs6663053	0.96[ASN][1000 genomes]
rs72675540	0.83[AMR][1000 genomes]
rs7534051	0.97[ASN][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	nsv870513	chr1:56407227-56493106	Weak transcription Enhancers ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	nsv1003385	chr1:56430742-56468732	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:56457600-56463200	Weak transcription	Colon Smooth Muscle	Colon
2	chr1:56460200-56463200	Weak transcription	NHDF-Ad	bronchial

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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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