Variant report

Variant	rs4922523
Chromosome Location	chr10:48553511-48553512
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:8 , 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	chr10:48549200-48554200	Weak transcription	Esophagus	oesophagus
4	chr10:48549600-48554800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr10:48551400-48554600	Weak transcription	NHEK	skin
6	chr10:48551400-48557000	Weak transcription	Primary T cells from cord blood	blood
7	chr10:48551800-48554400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
8	chr10:48551800-48563200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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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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