Variant report

Variant	rs73943916
Chromosome Location	chr2:86166389-86166390
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:11 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:86160800-86166800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
2	chr2:86164200-86169200	Weak transcription	Pancreas	Pancrea
3	chr2:86164200-86169400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr2:86164600-86166800	Enhancers	Liver	Liver
5	chr2:86164800-86168400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
6	chr2:86165000-86167600	Weak transcription	Spleen	Spleen
7	chr2:86165200-86166400	Enhancers	HUVEC	blood vessel
8	chr2:86166000-86166800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
9	chr2:86166000-86167600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
10	chr2:86166200-86166400	Weak transcription	A549	lung
11	chr2:86166200-86166600	Enhancers	Ovary	ovary

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