Variant report

Variant	rs185317529
Chromosome Location	chr3:70550746-70550747
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	nsv999046	chr3:70549472-70576944	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:70549800-70551800	Enhancers	Fetal Thymus	thymus
2	chr3:70550000-70551400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
3	chr3:70550400-70551200	Enhancers	Dnd41	blood
4	chr3:70550600-70551000	Enhancers	Primary hematopoietic stem cells	blood
5	chr3:70550600-70551000	Enhancers	Primary hematopoietic stem cells short term culture	blood
6	chr3:70550600-70551600	Enhancers	Primary B cells from cord blood	blood

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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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