Variant report

Variant rs191169627
Chromosome Location chr19:43629577-43629578
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr19:43625200-43629600 Weak transcription Osteobl bone
2 chr19:43625200-43630800 Weak transcription NHLF lung
3 chr19:43625200-43631000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
4 chr19:43625400-43630800 Weak transcription Muscle Satellite Cultured Cells --
5 chr19:43626200-43630200 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
6 chr19:43626200-43630800 Weak transcription Breast Myoepithelial Primary Cells Breast
7 chr19:43626200-43631000 Weak transcription Brain Inferior Temporal Lobe brain
8 chr19:43627000-43630800 Weak transcription NHDF-Ad bronchial
9 chr19:43627800-43636000 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
10 chr19:43628000-43630800 Weak transcription Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
11 chr19:43628400-43630000 Enhancers Placenta Placenta
12 chr19:43628800-43630800 Weak transcription HMEC breast
13 chr19:43629000-43630000 Weak transcription NHEK skin
14 chr19:43629400-43630800 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung

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