Variant report

Variant rs34319089
Chromosome Location chr14:32138101-32138102
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr14:32117000-32148200 Weak transcription Pancreas Pancrea
2 chr14:32135200-32147000 Weak transcription Fetal Adrenal Gland Adrenal Gland
3 chr14:32135400-32147000 Weak transcription HepG2 liver
4 chr14:32135800-32170800 Weak transcription Primary T helper naive cells fromperipheralblood blood
5 chr14:32136000-32144200 Weak transcription Skeletal Muscle Female skeletal muscle
6 chr14:32136200-32147000 Weak transcription Fetal Stomach stomach
7 chr14:32137000-32138200 ZNF genes & repeats Primary hematopoietic stem cells G-CSF-mobilized Male --
8 chr14:32137000-32146800 Weak transcription Spleen Spleen
9 chr14:32137200-32138200 ZNF genes & repeats Fetal Intestine Small intestine
10 chr14:32137200-32147000 Weak transcription Skeletal Muscle Male skeletal muscle
11 chr14:32137200-32147400 Weak transcription Left Ventricle heart
12 chr14:32137200-32149400 Weak transcription Primary T killer naive cells fromperipheralblood blood
13 chr14:32137600-32138200 Strong transcription H1 Derived Mesenchymal Stem Cells ES cell derived
14 chr14:32137600-32146800 Weak transcription Primary mononuclear cells fromperipheralblood Blood
15 chr14:32137800-32138200 ZNF genes & repeats Lung lung

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