Variant report

Variant rs72901422
Chromosome Location chr11:45445336-45445337
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr11:45436400-45456800 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
2 chr11:45444600-45445400 Bivalent Enhancer Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
3 chr11:45444600-45447800 Enhancers Fetal Brain Male brain
4 chr11:45444800-45445400 Enhancers Left Ventricle heart
5 chr11:45444800-45445400 Enhancers Lung lung
6 chr11:45444800-45445400 Enhancers HSMMtube muscle
7 chr11:45444800-45446200 Enhancers Fetal Heart heart
8 chr11:45445000-45445400 Enhancers Stomach Smooth Muscle stomach
9 chr11:45445000-45445600 Enhancers Brain Cingulate Gyrus brain
10 chr11:45445000-45446000 Enhancers Brain Germinal Matrix brain
11 chr11:45445000-45446000 Enhancers Brain Substantia Nigra brain
12 chr11:45445000-45446000 Enhancers Colon Smooth Muscle Colon
13 chr11:45445000-45446000 Enhancers Right Ventricle heart
14 chr11:45445000-45447200 Enhancers Fetal Brain Female brain
15 chr11:45445000-45449600 Weak transcription Spleen Spleen
16 chr11:45445200-45445600 Enhancers Ganglion Eminence derived primary cultured neurospheres brain
17 chr11:45445200-45446400 Enhancers Fetal Stomach stomach
18 chr11:45445200-45446600 Weak transcription Aorta Aorta

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