Variant report

Variant rs28515738
Chromosome Location chr14:104663412-104663413
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr14:104656200-104669200 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
2 chr14:104657200-104665400 Weak transcription Fetal Brain Female brain
3 chr14:104661400-104663600 Bivalent Enhancer Fetal Muscle Trunk muscle
4 chr14:104662000-104663800 Enhancers Fetal Brain Male brain
5 chr14:104662000-104664000 Enhancers Fetal Lung lung
6 chr14:104662200-104663600 Bivalent Enhancer Fetal Stomach stomach
7 chr14:104662400-104663600 Enhancers Primary B cells from peripheral blood blood
8 chr14:104662800-104663600 Bivalent Enhancer Fetal Adrenal Gland Adrenal Gland
9 chr14:104663000-104663600 Enhancers Ovary ovary
10 chr14:104663000-104663600 Enhancers Pancreas Pancrea
11 chr14:104663200-104668400 Weak transcription Gastric stomach
12 chr14:104663200-104672400 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
13 chr14:104663400-104665600 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
14 chr14:104663400-104667400 Weak transcription Spleen Spleen
15 chr14:104663400-104668800 Enhancers Brain Germinal Matrix brain

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