Variant report

Variant rs556092330
Chromosome Location chr2:40165142-40165143
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:40147000-40167400 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
2 chr2:40164600-40166400 Flanking Active TSS Dnd41 blood
3 chr2:40164800-40166000 Enhancers Primary hematopoietic stem cells short term culture blood
4 chr2:40164800-40166200 Enhancers Fetal Thymus thymus
5 chr2:40164800-40166400 Enhancers IMR90 fetal lung fibroblasts Cell Line lung
6 chr2:40164800-40166400 Enhancers HSMM muscle
7 chr2:40164800-40166400 Enhancers Osteobl bone
8 chr2:40165000-40165600 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
9 chr2:40165000-40166400 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
10 chr2:40165000-40166600 Enhancers Muscle Satellite Cultured Cells --
11 chr2:40165000-40166600 Enhancers NH-A brain
12 chr2:40165000-40166800 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
13 chr2:40165000-40175800 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin

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