Variant report

Variant	rs5998549
Chromosome Location	chr22:32993137-32993138
allele	C/T
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	chr22:32979400-32994200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr22:32981600-32996200	Weak transcription	HUES6 Cell Line	embryonic stem cell
3	chr22:32988000-32993200	Weak transcription	H9 Cell Line	embryonic stem cell
4	chr22:32989200-32998800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
5	chr22:32992000-32993200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
6	chr22:32992000-32993200	Enhancers	HMEC	breast
7	chr22:32992000-32993800	Enhancers	Breast Myoepithelial Primary Cells	Breast
8	chr22:32992200-32993200	Enhancers	NHEK	skin
9	chr22:32992400-32993200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
10	chr22:32993000-32999000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin

Quick Search:

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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