Variant report

Variant	rs536327927
Chromosome Location	chr1:172485544-172485545
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	nsv947551	chr1:172485154-172490045	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:172480800-172487800	Enhancers	Primary neutrophils fromperipheralblood	blood
2	chr1:172484400-172487600	Enhancers	Monocytes-CD14+_RO01746	blood
3	chr1:172484600-172487600	Enhancers	Primary monocytes fromperipheralblood	blood
4	chr1:172484600-172487800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
5	chr1:172484800-172487800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
6	chr1:172485200-172486800	Weak transcription	K562	blood
7	chr1:172485200-172488400	Weak transcription	Pancreatic Islets	Pancreatic Islet
8	chr1:172485400-172486200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
9	chr1:172485400-172486600	Weak transcription	Primary hematopoietic stem cells	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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