Variant report

Variant rs2584535
Chromosome Location chr9:17435459-17435460
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:17368400-17457800 Weak transcription Pancreas Pancrea
2 chr9:17396200-17440000 Weak transcription Adipose Nuclei Adipose
3 chr9:17408000-17437200 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
4 chr9:17411800-17435600 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
5 chr9:17411800-17439800 Weak transcription Left Ventricle heart
6 chr9:17411800-17481000 Weak transcription Aorta Aorta
7 chr9:17412200-17440200 Weak transcription Fetal Stomach stomach
8 chr9:17412200-17443600 Weak transcription Ovary ovary
9 chr9:17425400-17449600 Weak transcription Cortex derived primary cultured neurospheres brain
10 chr9:17426400-17466800 Weak transcription Primary hematopoietic stem cells blood
11 chr9:17428000-17435800 Weak transcription Liver Liver
12 chr9:17428600-17440200 Weak transcription Monocytes-CD14+_RO01746 blood
13 chr9:17431000-17453400 Weak transcription Fetal Lung lung
14 chr9:17434000-17437200 ZNF genes & repeats Primary hematopoietic stem cells G-CSF-mobilized Male --
15 chr9:17434000-17453600 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
16 chr9:17434000-17453600 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
17 chr9:17435400-17437000 Weak transcription Gastric stomach

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