Variant report

Variant	rs72896542
Chromosome Location	chr1:47687367-47687368
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:12 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:47674400-47690600	Weak transcription	Gastric	stomach
2	chr1:47679200-47689400	Weak transcription	Lung	lung
3	chr1:47679600-47689000	Weak transcription	Right Atrium	heart
4	chr1:47681800-47689600	Strong transcription	Primary hematopoietic stem cells short term culture	blood
5	chr1:47683600-47690000	Strong transcription	K562	blood
6	chr1:47683800-47690000	Strong transcription	HUVEC	blood vessel
7	chr1:47684600-47687400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
8	chr1:47684800-47687800	Strong transcription	Spleen	Spleen
9	chr1:47685000-47688000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
10	chr1:47685800-47687600	Strong transcription	Primary hematopoietic stem cells	blood
11	chr1:47686400-47690600	Weak transcription	Right Ventricle	heart
12	chr1:47687000-47687600	Strong transcription	Adipose Nuclei	Adipose

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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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