Variant report

Variant rs10266722
Chromosome Location chr7:40345582-40345583
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:12 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr7:40340000-40346400 Weak transcription NHDF-Ad bronchial
2 chr7:40340400-40346400 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
3 chr7:40340600-40346000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
4 chr7:40343000-40347200 Enhancers HUVEC blood vessel
5 chr7:40343000-40348000 Enhancers Muscle Satellite Cultured Cells --
6 chr7:40344400-40345800 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
7 chr7:40344400-40347400 Enhancers Osteobl bone
8 chr7:40344400-40348000 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
9 chr7:40344600-40347200 Enhancers HSMM muscle
10 chr7:40344600-40347200 Enhancers NH-A brain
11 chr7:40345000-40347600 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
12 chr7:40345200-40354800 Weak transcription HSMMtube muscle

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