Variant report

Variant rs7871205
Chromosome Location chr9:18982372-18982373
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:20 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:18979400-18982800 Enhancers Osteobl bone
2 chr9:18979800-18982400 Enhancers Fetal Heart heart
3 chr9:18979800-18983000 Enhancers Breast Myoepithelial Primary Cells Breast
4 chr9:18980400-18984400 Weak transcription Stomach Mucosa stomach
5 chr9:18981000-18982600 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
6 chr9:18981000-18983200 Enhancers NHDF-Ad bronchial
7 chr9:18981400-18982400 Enhancers Fetal Muscle Leg muscle
8 chr9:18981400-18982600 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
9 chr9:18981400-18982600 Enhancers Adipose Nuclei Adipose
10 chr9:18981400-18982600 Enhancers Colon Smooth Muscle Colon
11 chr9:18981600-18982400 Enhancers Ganglion Eminence derived primary cultured neurospheres brain
12 chr9:18981600-18982600 Enhancers H9 Derived Neuron Cultured Cells ES cell derived
13 chr9:18981600-18982600 Enhancers Fetal Thymus thymus
14 chr9:18981600-18984400 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
15 chr9:18981800-18982400 Enhancers Brain Anterior Caudate brain
16 chr9:18981800-18982800 Bivalent Enhancer Foreskin Keratinocyte Primary Cells skin02 Skin
17 chr9:18981800-18984800 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
18 chr9:18982000-18982600 Enhancers NHLF lung
19 chr9:18982200-18982600 Weak transcription Fetal Kidney kidney
20 chr9:18982200-18982800 Enhancers NHEK skin

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