Variant report

Variant	rs59225784
Chromosome Location	chr3:69197087-69197088
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 10 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs13321417	1.00[AMR][1000 genomes]
rs61737464	1.00[AMR][1000 genomes]
rs61737489	1.00[AMR][1000 genomes]
rs6766710	1.00[AMR][1000 genomes]
rs6796471	1.00[AMR][1000 genomes]
rs6806274	1.00[AMR][1000 genomes]
rs7626366	1.00[AMR][1000 genomes]
rs9757432	1.00[AMR][1000 genomes]
rs9850164	1.00[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	nsv876933	chr3:69059023-69227379	Enhancers Strong transcription Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	15 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:69194200-69198800	Weak transcription	Skeletal Muscle Male	skeletal muscle
2	chr3:69194400-69200600	Weak transcription	Psoas Muscle	Psoas
3	chr3:69195200-69197400	Weak transcription	Skeletal Muscle Female	skeletal muscle

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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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