Variant report

Variant	rs73194444
Chromosome Location	chr13:50405106-50405107
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:50396000-50414400	Weak transcription	Right Atrium	heart
2	chr13:50402200-50412800	Weak transcription	Fetal Intestine Small	intestine
3	chr13:50403000-50410200	Weak transcription	HepG2	liver
4	chr13:50404000-50410600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
5	chr13:50404400-50405600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
6	chr13:50404400-50406200	Enhancers	Primary hematopoietic stem cells short term culture	blood
7	chr13:50404400-50406200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
8	chr13:50404600-50405800	Enhancers	Primary hematopoietic stem cells	blood
9	chr13:50405000-50405400	Enhancers	Primary T regulatory 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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