Variant report

Variant rs10118602
Chromosome Location chr9:73450596-73450597
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:73427600-73483400 Weak transcription Aorta Aorta
2 chr9:73438600-73456800 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
3 chr9:73442200-73459800 Weak transcription HUES64 Cell Line embryonic stem cell
4 chr9:73443000-73453400 Weak transcription Breast Myoepithelial Primary Cells Breast
5 chr9:73448200-73454800 Weak transcription Gastric stomach
6 chr9:73448200-73473600 Weak transcription Fetal Kidney kidney
7 chr9:73448400-73459200 Weak transcription Ganglion Eminence derived primary cultured neurospheres brain
8 chr9:73448400-73469000 Weak transcription Muscle Satellite Cultured Cells --
9 chr9:73448600-73457000 Weak transcription Cortex derived primary cultured neurospheres brain
10 chr9:73449200-73451400 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
11 chr9:73449200-73455400 Weak transcription hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
12 chr9:73449400-73450600 Enhancers NHDF-Ad bronchial
13 chr9:73449400-73455200 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
14 chr9:73449600-73450600 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
15 chr9:73449600-73453400 Weak transcription H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
16 chr9:73450400-73450600 Enhancers Ovary ovary

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