Variant report

Variant rs10962960
Chromosome Location chr9:17262401-17262402
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:17223600-17279400 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
2 chr9:17247400-17269000 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
3 chr9:17259200-17262800 Weak transcription Fetal Brain Male brain
4 chr9:17260600-17269000 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
5 chr9:17261600-17262800 ZNF genes & repeats Primary hematopoietic stem cells G-CSF-mobilized Male --
6 chr9:17261600-17262800 ZNF genes & repeats Ganglion Eminence derived primary cultured neurospheres brain
7 chr9:17261800-17262600 ZNF genes & repeats Liver Liver
8 chr9:17261800-17262800 ZNF genes & repeats Adipose Nuclei Adipose
9 chr9:17262000-17262800 ZNF genes & repeats Cortex derived primary cultured neurospheres brain
10 chr9:17262000-17262800 ZNF genes & repeats Fetal Lung lung
11 chr9:17262000-17262800 ZNF genes & repeats Ovary ovary
12 chr9:17262400-17262800 ZNF genes & repeats IMR90 fetal lung fibroblasts Cell Line lung
13 chr9:17262400-17262800 ZNF genes & repeats Left Ventricle heart
14 chr9:17262400-17263000 ZNF genes & repeats Dnd41 blood

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