Variant report

Variant	rs9421763
Chromosome Location	chr10:48556423-48556424
allele	A/G
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	chr10:48540800-48562800	Weak transcription	Right Atrium	heart
2	chr10:48544000-48557400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr10:48551400-48557000	Weak transcription	Primary T cells from cord blood	blood
4	chr10:48551800-48563200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr10:48555000-48557000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
6	chr10:48555200-48557400	Enhancers	HepG2	liver
7	chr10:48555800-48560200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
8	chr10:48556200-48556800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
9	chr10:48556200-48557000	Enhancers	Fetal Lung	lung
10	chr10:48556200-48557000	Weak transcription	Stomach Smooth Muscle	stomach
11	chr10:48556200-48557600	Weak transcription	Fetal Stomach	stomach
12	chr10:48556400-48556800	Weak transcription	Pancreas	Pancrea

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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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