Variant report

Variant	rs12794546
Chromosome Location	chr11:121062593-121062594
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:12 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:121052800-121065600	Weak transcription	Gastric	stomach
2	chr11:121053800-121065600	Weak transcription	Pancreas	Pancrea
3	chr11:121055400-121065600	Weak transcription	Ovary	ovary
4	chr11:121055600-121065600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr11:121056800-121065400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
6	chr11:121056800-121065600	Weak transcription	Skeletal Muscle Male	skeletal muscle
7	chr11:121058000-121065400	Weak transcription	Fetal Lung	lung
8	chr11:121058600-121062600	Weak transcription	Brain Cingulate Gyrus	brain
9	chr11:121058800-121069000	Weak transcription	HUES6 Cell Line	embryonic stem cell
10	chr11:121061600-121062600	Enhancers	HSMMtube	muscle
11	chr11:121061800-121062600	Enhancers	Fetal Heart	heart
12	chr11:121061800-121063200	Enhancers	Right Atrium	heart

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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