Variant report

Variant	rs56326427
Chromosome Location	chr9:117545637-117545638
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:17 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:117539200-117548200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr9:117542000-117547200	Weak transcription	Lung	lung
3	chr9:117542000-117547400	Weak transcription	Adipose Nuclei	Adipose
4	chr9:117542000-117547800	Weak transcription	Esophagus	oesophagus
5	chr9:117542000-117548000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
6	chr9:117542000-117561800	Weak transcription	Pancreas	Pancrea
7	chr9:117542400-117549800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
8	chr9:117542400-117552600	Weak transcription	Duodenum Mucosa	Duodenum
9	chr9:117542400-117561200	Weak transcription	Rectal Mucosa Donor 31	rectum
10	chr9:117542800-117560200	Weak transcription	A549	lung
11	chr9:117543000-117550400	Weak transcription	Fetal Intestine Small	intestine
12	chr9:117543200-117548400	Weak transcription	Hela-S3	cervix
13	chr9:117543200-117551200	Weak transcription	Fetal Intestine Large	intestine
14	chr9:117543200-117552400	Weak transcription	HUVEC	blood vessel
15	chr9:117543600-117548200	Weak transcription	Stomach Mucosa	stomach
16	chr9:117545400-117561400	Weak transcription	Gastric	stomach
17	chr9:117545600-117546000	Weak transcription	Primary B cells from peripheral blood	blood

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