Variant report

Variant rs373212770
Chromosome Location chr14:104669513-104669514
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr14:104663200-104672400 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
2 chr14:104664200-104669600 Enhancers Fetal Brain Male brain
3 chr14:104665400-104669600 Enhancers Fetal Brain Female brain
4 chr14:104667600-104673000 Weak transcription Spleen Spleen
5 chr14:104667800-104669800 Bivalent Enhancer Fetal Muscle Trunk muscle
6 chr14:104668400-104670000 Bivalent Enhancer Fetal Muscle Leg muscle
7 chr14:104669000-104672600 Weak transcription Brain Inferior Temporal Lobe brain
8 chr14:104669000-104672600 Weak transcription Gastric stomach
9 chr14:104669000-104672600 Weak transcription Pancreas Pancrea
10 chr14:104669000-104672600 Weak transcription Rectal Mucosa Donor 29 rectum
11 chr14:104669200-104669800 ZNF genes & repeats H1 Derived Mesenchymal Stem Cells ES cell derived
12 chr14:104669200-104672400 Weak transcription Fetal Lung lung
13 chr14:104669400-104669600 Enhancers Brain Germinal Matrix brain
14 chr14:104669400-104669600 Bivalent Enhancer Skeletal Muscle Male skeletal muscle

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