Variant report

Variant rs2214611
Chromosome Location chr19:43627851-43627852
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr19:43624000-43628400 Weak transcription Placenta Placenta
2 chr19:43625200-43629600 Weak transcription Osteobl bone
3 chr19:43625200-43630800 Weak transcription NHLF lung
4 chr19:43625200-43631000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
5 chr19:43625400-43630800 Weak transcription Muscle Satellite Cultured Cells --
6 chr19:43626200-43630200 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
7 chr19:43626200-43630800 Weak transcription Breast Myoepithelial Primary Cells Breast
8 chr19:43626200-43631000 Weak transcription Brain Inferior Temporal Lobe brain
9 chr19:43626800-43628400 Weak transcription HMEC breast
10 chr19:43627000-43628400 Weak transcription NHEK skin
11 chr19:43627000-43630800 Weak transcription NHDF-Ad bronchial
12 chr19:43627400-43628000 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
13 chr19:43627800-43629400 Enhancers IMR90 fetal lung fibroblasts Cell Line lung
14 chr19:43627800-43636000 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin

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