Variant report

Variant rs73668349
Chromosome Location chr9:139534857-139534858
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:21 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:139526000-139535000 Weak transcription Right Atrium heart
2 chr9:139526000-139535000 Weak transcription Right Ventricle heart
3 chr9:139526000-139538000 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
4 chr9:139526000-139538200 Weak transcription Gastric stomach
5 chr9:139526200-139535200 Weak transcription Lung lung
6 chr9:139526400-139535800 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Male --
7 chr9:139532600-139535000 Weak transcription HSMMtube muscle
8 chr9:139532600-139535200 Weak transcription HSMM muscle
9 chr9:139532600-139538600 Weak transcription Pancreas Pancrea
10 chr9:139532600-139538800 Weak transcription Brain Inferior Temporal Lobe brain
11 chr9:139533000-139535000 Weak transcription Skeletal Muscle Female skeletal muscle
12 chr9:139534200-139536000 Enhancers Spleen Spleen
13 chr9:139534400-139535800 Enhancers Fetal Adrenal Gland Adrenal Gland
14 chr9:139534600-139535600 Enhancers Fetal Muscle Leg muscle
15 chr9:139534600-139535800 Enhancers Left Ventricle heart
16 chr9:139534600-139536800 Enhancers Adipose Nuclei Adipose
17 chr9:139534800-139535000 Bivalent Enhancer Foreskin Keratinocyte Primary Cells skin02 Skin
18 chr9:139534800-139535000 Bivalent Enhancer Skeletal Muscle Male skeletal muscle
19 chr9:139534800-139535200 Bivalent Enhancer Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
20 chr9:139534800-139535200 Bivalent Enhancer Fetal Muscle Trunk muscle
21 chr9:139534800-139535600 Enhancers K562 blood

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