Variant report

Variant	rs73509652
Chromosome Location	chr9:93895609-93895610
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:11 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:93882400-93898600	Weak transcription	Stomach Mucosa	stomach
2	chr9:93893400-93906000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
3	chr9:93893800-93896000	Enhancers	Muscle Satellite Cultured Cells	--
4	chr9:93894400-93900800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr9:93894600-93896800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
6	chr9:93894600-93896800	Weak transcription	A549	lung
7	chr9:93894600-93896800	Weak transcription	NHEK	skin
8	chr9:93894600-93901000	Weak transcription	HMEC	breast
9	chr9:93894800-93895800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
10	chr9:93894800-93900800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
11	chr9:93895200-93896800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	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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