Variant report

Variant	rs189692494
Chromosome Location	chr15:73191064-73191065
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 3 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv977733	chr15:73189238-73192771	Enhancers Weak transcription	TF binding region lncRNA	1 gene(s)	inside rSNPs	n/a
2	esv3444494	chr15:73189724-73192272	Enhancers Weak transcription	lncRNA	n/a	inside rSNPs	n/a
3	esv3366971	chr15:73189999-73191947	Enhancers Weak transcription	lncRNA	n/a	inside rSNPs	n/a

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:73190400-73192200	Weak transcription	Aorta	Aorta
2	chr15:73190400-73194000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow

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

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