Variant report

Variant rs1899505
Chromosome Location chr11:27140763-27140764
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr11:27137200-27144600 Weak transcription Brain Substantia Nigra brain
2 chr11:27138000-27141800 Enhancers Muscle Satellite Cultured Cells --
3 chr11:27138000-27142000 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
4 chr11:27138000-27142000 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
5 chr11:27138000-27142200 Enhancers Osteobl bone
6 chr11:27138000-27142400 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
7 chr11:27138400-27141800 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
8 chr11:27139600-27143200 Weak transcription Breast Myoepithelial Primary Cells Breast
9 chr11:27140000-27142000 Enhancers NHDF-Ad bronchial
10 chr11:27140400-27141000 Enhancers H9 Derived Neuron Cultured Cells ES cell derived
11 chr11:27140600-27140800 Enhancers Fetal Adrenal Gland Adrenal Gland
12 chr11:27140600-27141000 Enhancers iPS-18 Cell Line embryonic stem cell
13 chr11:27140600-27141000 Enhancers Aorta Aorta
14 chr11:27140600-27141600 Weak transcription Liver Liver

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