Variant report

Variant	rs876800
Chromosome Location	chr2:180444337-180444338
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:14 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:180433000-180445600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr2:180435200-180461000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr2:180435400-180446400	Weak transcription	Fetal Kidney	kidney
4	chr2:180437600-180445200	Weak transcription	Skeletal Muscle Male	skeletal muscle
5	chr2:180439400-180445000	Weak transcription	Stomach Mucosa	stomach
6	chr2:180439800-180445200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
7	chr2:180439800-180445200	Weak transcription	Fetal Lung	lung
8	chr2:180439800-180446400	Enhancers	Liver	Liver
9	chr2:180441200-180445200	Weak transcription	Pancreas	Pancrea
10	chr2:180442400-180446800	Enhancers	HepG2	liver
11	chr2:180443600-180444600	Weak transcription	Fetal Intestine Small	intestine
12	chr2:180443600-180445000	Weak transcription	Fetal Intestine Large	intestine
13	chr2:180444200-180445200	Weak transcription	Pancreatic Islets	Pancreatic Islet
14	chr2:180444200-180445800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte 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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