Variant report

Variant rs12462607
Chromosome Location chr19:43632017-43632018
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr19:43627800-43636000 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
2 chr19:43630000-43633600 Enhancers NHEK skin
3 chr19:43630200-43636000 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
4 chr19:43630600-43632600 Enhancers Osteobl bone
5 chr19:43630800-43632200 Enhancers NH-A brain
6 chr19:43630800-43632400 Enhancers Muscle Satellite Cultured Cells --
7 chr19:43630800-43632600 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
8 chr19:43630800-43632800 Enhancers NHLF lung
9 chr19:43630800-43633200 Enhancers NHDF-Ad bronchial
10 chr19:43630800-43636000 Enhancers Breast Myoepithelial Primary Cells Breast
11 chr19:43630800-43636200 Enhancers HMEC breast
12 chr19:43631000-43632200 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
13 chr19:43631000-43632200 Enhancers HSMM muscle
14 chr19:43631000-43632400 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
15 chr19:43631000-43632600 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
16 chr19:43631600-43637000 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
17 chr19:43631800-43633000 Weak transcription Placenta Placenta
18 chr19:43632000-43632800 Enhancers A549 lung

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