Variant report

Variant	rs2138194
Chromosome Location	chr2:180502186-180502187
allele	C/G
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	chr2:180495000-180502200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr2:180500800-180502400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
3	chr2:180500800-180502400	Enhancers	Liver	Liver
4	chr2:180501000-180502400	Enhancers	Fetal Lung	lung
5	chr2:180501000-180502400	Enhancers	Skeletal Muscle Male	skeletal muscle
6	chr2:180501000-180502400	Enhancers	Skeletal Muscle Female	skeletal muscle
7	chr2:180501000-180502600	Enhancers	HSMMtube	muscle
8	chr2:180501200-180502200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
9	chr2:180501400-180502200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
10	chr2:180501600-180502400	Enhancers	Fetal Heart	heart
11	chr2:180501600-180502400	Enhancers	HepG2	liver

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