Variant report

Variant	rs13433062
Chromosome Location	chr2:20301300-20301301
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	chr2:20293600-20304200	Weak transcription	Stomach Mucosa	stomach
2	chr2:20294000-20304400	Weak transcription	Pancreas	Pancrea
3	chr2:20298000-20303000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr2:20298400-20307800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr2:20299600-20301800	Enhancers	Placenta	Placenta
6	chr2:20299800-20301400	Enhancers	HepG2	liver
7	chr2:20300000-20303600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
8	chr2:20301200-20306400	Weak transcription	HUVEC	blood vessel

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

what's new

Quick links