Variant report

Variant	rs537105812
Chromosome Location	chr12:103848279-103848280
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 2 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3338592	chr12:103817534-103849094	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
2	esv3383576	chr12:103847913-103848291	Enhancers	Chromatin interactive region	n/a	inside rSNPs	n/a

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:103847600-103851400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
2	chr12:103847800-103849000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
3	chr12:103847800-103850600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
4	chr12:103848000-103851400	Enhancers	Primary T helper naive cells fromperipheralblood	blood
5	chr12:103848200-103850600	Enhancers	Primary T helper naive cells from peripheral blood	blood
6	chr12:103848200-103851800	Enhancers	Primary B cells from peripheral 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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