Variant report

Variant	rs9792678
Chromosome Location	chr9:93968640-93968641
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:18 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:93959800-93969600	Weak transcription	Gastric	stomach
2	chr9:93961000-93969400	Weak transcription	Osteobl	bone
3	chr9:93961000-93969800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
4	chr9:93961200-93969200	Weak transcription	Liver	Liver
5	chr9:93961200-93969600	Weak transcription	Right Atrium	heart
6	chr9:93961200-93975600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
7	chr9:93962400-93969800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
8	chr9:93962400-93969800	Weak transcription	K562	blood
9	chr9:93962600-93969600	Weak transcription	Stomach Mucosa	stomach
10	chr9:93963200-93969800	Weak transcription	Rectal Mucosa Donor 29	rectum
11	chr9:93965200-93968800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
12	chr9:93965400-93968800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
13	chr9:93965400-93969600	Weak transcription	Fetal Lung	lung
14	chr9:93965400-93969600	Weak transcription	Psoas Muscle	Psoas
15	chr9:93965800-93969400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
16	chr9:93968000-93969800	Enhancers	HepG2	liver
17	chr9:93968600-93968800	Enhancers	Breast Myoepithelial Primary Cells	Breast
18	chr9:93968600-93971400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin

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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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