Variant report

Variant rs10143462
Chromosome Location chr14:104665730-104665731
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr14:104656200-104669200 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
2 chr14:104663200-104668400 Weak transcription Gastric stomach
3 chr14:104663200-104672400 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
4 chr14:104663400-104667400 Weak transcription Spleen Spleen
5 chr14:104663400-104668800 Enhancers Brain Germinal Matrix brain
6 chr14:104663600-104668000 Weak transcription Pancreas Pancrea
7 chr14:104664000-104668400 Weak transcription Fetal Lung lung
8 chr14:104664200-104669600 Enhancers Fetal Brain Male brain
9 chr14:104665400-104669600 Enhancers Fetal Brain Female brain
10 chr14:104665600-104665800 Bivalent Enhancer Cortex derived primary cultured neurospheres brain
11 chr14:104665600-104665800 Bivalent Enhancer Brain Inferior Temporal Lobe brain
12 chr14:104665600-104665800 Bivalent Enhancer Fetal Muscle Trunk muscle
13 chr14:104665600-104666000 Enhancers iPS DF 19.11 Cell Line embryonic stem cell
14 chr14:104665600-104666000 Bivalent Enhancer Fetal Muscle Leg muscle

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