Variant report

Variant rs539675038
Chromosome Location chr9:496131-496132
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:489600-503200 Weak transcription Breast Myoepithelial Primary Cells Breast
2 chr9:494400-496200 Enhancers A549 lung
3 chr9:494400-496200 Enhancers HepG2 liver
4 chr9:494400-496400 Enhancers Stomach Mucosa stomach
5 chr9:494600-496200 Enhancers H9 Derived Neuron Cultured Cells ES cell derived
6 chr9:494600-496400 Enhancers Pancreas Pancrea
7 chr9:495000-496200 Enhancers H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
8 chr9:495200-496200 Enhancers H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
9 chr9:495400-496200 Enhancers hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
10 chr9:495400-496200 Enhancers Fetal Adrenal Gland Adrenal Gland
11 chr9:495600-496200 Enhancers H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
12 chr9:495800-496200 Enhancers Gastric stomach
13 chr9:495800-503200 Weak transcription ES-UCSF4 Cell Line embryonic stem cell

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