Variant report

Variant rs74088547
Chromosome Location chr14:104820616-104820617
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:20 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr14:104819600-104820800 Bivalent Enhancer Right Ventricle heart
2 chr14:104819800-104821000 Enhancers Ganglion Eminence derived primary cultured neurospheres brain
3 chr14:104819800-104822000 Bivalent Enhancer Fetal Stomach stomach
4 chr14:104820000-104823400 Enhancers Brain Germinal Matrix brain
5 chr14:104820000-104823600 Enhancers Fetal Muscle Leg muscle
6 chr14:104820000-104824200 Bivalent Enhancer Fetal Muscle Trunk muscle
7 chr14:104820200-104821000 Bivalent Enhancer Adipose Nuclei Adipose
8 chr14:104820200-104821000 Bivalent Enhancer Skeletal Muscle Male skeletal muscle
9 chr14:104820200-104822400 Enhancers Left Ventricle heart
10 chr14:104820200-104823000 Bivalent Enhancer Fetal Adrenal Gland Adrenal Gland
11 chr14:104820400-104821000 Enhancers Cortex derived primary cultured neurospheres brain
12 chr14:104820400-104821000 Bivalent Enhancer Brain Dorsolateral Prefrontal Cortex brain
13 chr14:104820400-104821000 Enhancers Lung lung
14 chr14:104820400-104821600 Enhancers iPS DF 19.11 Cell Line embryonic stem cell
15 chr14:104820400-104821600 Weak transcription Spleen Spleen
16 chr14:104820400-104822600 Enhancers Fetal Lung lung
17 chr14:104820400-104822800 Enhancers Fetal Brain Male brain
18 chr14:104820600-104821000 Bivalent Enhancer H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
19 chr14:104820600-104821000 Bivalent Enhancer Primary T cells fromperipheralblood blood
20 chr14:104820600-104821000 Enhancers Fetal Brain Female brain

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