Variant report

Variant	rs546390722
Chromosome Location	chr7:147416953-147416954
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 1 )
Associated
traits (count: 0)

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	nsv824373	chr7:147416397-147417121	Weak transcription Enhancers	n/a	n/a	inside rSNPs	n/a

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:147414200-147419000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
2	chr7:147414200-147419400	Weak transcription	Primary hematopoietic stem cells	blood
3	chr7:147416600-147417200	Enhancers	Brain Anterior Caudate	brain
4	chr7:147416800-147417600	Enhancers	Brain Substantia Nigra	brain

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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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