Variant report

Variant	rs16990824
Chromosome Location	chr22:32999059-32999060
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:15 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr22:32993800-33001200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
2	chr22:32997800-33000600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr22:32998000-32999200	Enhancers	K562	blood
4	chr22:32998200-32999200	Enhancers	Fetal Heart	heart
5	chr22:32998800-32999200	Flanking Active TSS	Hela-S3	cervix
6	chr22:32998800-32999200	Enhancers	HSMMtube	muscle
7	chr22:32998800-32999200	Enhancers	NHEK	skin
8	chr22:32998800-32999800	Enhancers	HMEC	breast
9	chr22:32998800-33004000	Enhancers	Placenta	Placenta
10	chr22:32999000-32999200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
11	chr22:32999000-32999200	Enhancers	Fetal Muscle Leg	muscle
12	chr22:32999000-32999400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
13	chr22:32999000-32999800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
14	chr22:32999000-32999800	Enhancers	Left Ventricle	heart
15	chr22:32999000-33000600	Enhancers	Right Atrium	heart

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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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