Variant report

Variant	rs9658294
Chromosome Location	chr12:117756491-117756492
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	chr12:117728000-117771200	Weak transcription	Skeletal Muscle Female	skeletal muscle
2	chr12:117739800-117771400	Weak transcription	Skeletal Muscle Male	skeletal muscle
3	chr12:117749400-117770800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr12:117756000-117756800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr12:117756200-117756800	Enhancers	Breast Myoepithelial Primary Cells	Breast
6	chr12:117756400-117756600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
7	chr12:117756400-117756800	Enhancers	Fetal Muscle Trunk	muscle
8	chr12:117756400-117757000	Enhancers	NHEK	skin
9	chr12:117756400-117757200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin

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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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