Variant report

Variant rs11626536
Chromosome Location chr14:32291088-32291089
allele A/C
Outlinks Ensembl   UCSC
Chromatin state (count:11 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr14:32250600-32322400 Weak transcription Primary T helper cells fromperipheralblood blood
2 chr14:32280000-32292200 Weak transcription Fetal Adrenal Gland Adrenal Gland
3 chr14:32281800-32330200 Weak transcription Primary T helper naive cells fromperipheralblood blood
4 chr14:32282600-32298000 Weak transcription Fetal Stomach stomach
5 chr14:32288400-32298200 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
6 chr14:32288800-32295800 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
7 chr14:32289200-32298200 Weak transcription Placenta Placenta
8 chr14:32290600-32291200 Enhancers H9 Derived Neuron Cultured Cells ES cell derived
9 chr14:32291000-32291400 Enhancers Brain Germinal Matrix brain
10 chr14:32291000-32299600 Weak transcription Brain Anterior Caudate brain
11 chr14:32291000-32310400 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin

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