Variant report

Variant rs72684978
Chromosome Location chr9:18261065-18261066
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:18256200-18261200 Weak transcription Duodenum Smooth Muscle Duodenum
2 chr9:18256800-18265200 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
3 chr9:18257000-18267200 Weak transcription NHDF-Ad bronchial
4 chr9:18260000-18261800 Enhancers Colon Smooth Muscle Colon
5 chr9:18260200-18261400 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
6 chr9:18260200-18261400 Enhancers Osteobl bone
7 chr9:18260200-18261600 Enhancers Ganglion Eminence derived primary cultured neurospheres brain
8 chr9:18260200-18261800 Enhancers HSMM muscle
9 chr9:18260200-18262400 Enhancers HMEC breast
10 chr9:18260400-18261400 Enhancers Breast Myoepithelial Primary Cells Breast
11 chr9:18260400-18261400 Flanking Active TSS Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
12 chr9:18260400-18261400 Enhancers Fetal Heart heart
13 chr9:18260400-18261800 Enhancers Fetal Stomach stomach
14 chr9:18260600-18261400 Enhancers Fetal Adrenal Gland Adrenal Gland
15 chr9:18260800-18261200 Enhancers hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
16 chr9:18260800-18261400 Enhancers Fetal Lung lung
17 chr9:18260800-18261800 Enhancers hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
18 chr9:18261000-18261400 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast

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