Variant report

Variant	rs191707396
Chromosome Location	chr19:42319347-42319348
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	nsv522854	chr19:42120283-42931004	Weak transcription Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Active TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	104 gene(s)	inside rSNPs	diseases
2	nsv960847	chr19:42319253-42339596	Enhancers Bivalent Enhancer Weak transcription Genic enhancers	TF binding region Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:42318200-42319600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
2	chr19:42318600-42319400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
3	chr19:42318600-42319800	Enhancers	Primary hematopoietic stem cells short term culture	blood
4	chr19:42318800-42319400	Enhancers	Primary T helper naive cells fromperipheralblood	blood
5	chr19:42318800-42319600	Enhancers	Primary hematopoietic stem cells	blood
6	chr19:42319000-42322800	Weak transcription	Primary neutrophils 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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