Variant report

Variant rs7033974
Chromosome Location chr9:17249636-17249637
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 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 chr9:17229800-17251600 Weak transcription HSMM muscle
3 chr9:17236400-17262000 Weak transcription Ovary ovary
4 chr9:17241000-17249800 Weak transcription Fetal Heart heart
5 chr9:17247200-17251000 Weak transcription Fetal Kidney kidney
6 chr9:17247400-17269000 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
7 chr9:17248000-17250800 Weak transcription Left Ventricle heart
8 chr9:17249400-17249800 ZNF genes & repeats Right Ventricle heart
9 chr9:17249600-17250200 ZNF genes & repeats Cortex derived primary cultured neurospheres brain
10 chr9:17249600-17250200 ZNF genes & repeats Foreskin Melanocyte Primary Cells skin03 Skin
11 chr9:17249600-17252000 ZNF genes & repeats Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
12 chr9:17249600-17252400 ZNF genes & repeats Liver Liver
13 chr9:17249600-17252400 ZNF genes & repeats Fetal Lung lung
14 chr9:17249600-17253000 ZNF genes & repeats Monocytes-CD14+_RO01746 blood
15 chr9:17249600-17254600 ZNF genes & repeats Primary hematopoietic stem cells G-CSF-mobilized Male --

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