Variant report

Variant	rs5998552
Chromosome Location	chr22:32995957-32995958
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr22:32981600-32996200	Weak transcription	HUES6 Cell Line	embryonic stem cell
2	chr22:32989200-32998800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
3	chr22:32993000-32999000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
4	chr22:32993200-32998600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
5	chr22:32993200-32998800	Weak transcription	HMEC	breast
6	chr22:32993200-32998800	Weak transcription	NHEK	skin
7	chr22:32993800-33001200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
8	chr22:32995600-32996000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
9	chr22:32995600-32996600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
10	chr22:32995800-32996600	Enhancers	Placenta	Placenta

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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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