Variant report

Variant rs56899761
Chromosome Location chr3:100922145-100922146
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:19 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr3:100913200-100922200 Weak transcription NHLF lung
2 chr3:100915600-100922200 Weak transcription Colon Smooth Muscle Colon
3 chr3:100919600-100922200 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
4 chr3:100919600-100923200 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
5 chr3:100919600-100924000 Weak transcription Fetal Adrenal Gland Adrenal Gland
6 chr3:100920400-100924000 Weak transcription Fetal Lung lung
7 chr3:100921600-100922600 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Male --
8 chr3:100921600-100925600 Enhancers Breast Myoepithelial Primary Cells Breast
9 chr3:100921800-100923400 Enhancers Muscle Satellite Cultured Cells --
10 chr3:100922000-100922600 Enhancers NH-A brain
11 chr3:100922000-100922600 Enhancers Osteobl bone
12 chr3:100922000-100923000 Enhancers HSMM muscle
13 chr3:100922000-100923200 Enhancers HMEC breast
14 chr3:100922000-100923400 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
15 chr3:100922000-100923400 Enhancers HSMMtube muscle
16 chr3:100922000-100923600 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
17 chr3:100922000-100923600 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
18 chr3:100922000-100924200 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
19 chr3:100922000-100924200 Enhancers NHEK skin

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