Variant report

Variant	rs532962921
Chromosome Location	chr10:94550730-94550731
allele	C/T
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	esv3372373	chr10:94550554-94550818	Enhancers Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	n/a

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:94546600-94551200	Enhancers	Primary B cells from peripheral blood	blood
2	chr10:94546800-94551200	Enhancers	Primary B cells from cord blood	blood
3	chr10:94547000-94551400	Enhancers	Primary neutrophils fromperipheralblood	blood
4	chr10:94548600-94552000	Enhancers	Primary monocytes fromperipheralblood	blood
5	chr10:94549400-94551200	Enhancers	Primary hematopoietic stem cells	blood
6	chr10:94549600-94550800	Enhancers	Primary hematopoietic stem cells short term culture	blood
7	chr10:94549600-94550800	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
8	chr10:94550200-94550800	Enhancers	Primary Natural Killer cells fromperipheralblood	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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