Variant report

Variant rs559641630
Chromosome Location chr19:43321585-43321586
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr19:43321000-43321800 Enhancers A549 lung
2 chr19:43321000-43321800 Enhancers HMEC breast
3 chr19:43321000-43321800 Enhancers NHDF-Ad bronchial
4 chr19:43321400-43321800 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
5 chr19:43321400-43322800 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
6 chr19:43321400-43323000 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
7 chr19:43321400-43323000 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
8 chr19:43321400-43323000 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
9 chr19:43321400-43323000 Weak transcription NHEK skin
10 chr19:43321400-43323600 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
11 chr19:43321400-43323600 Weak transcription Muscle Satellite Cultured Cells --
12 chr19:43321400-43324000 Weak transcription Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
13 chr19:43321400-43324200 Weak transcription Cortex derived primary cultured neurospheres brain
14 chr19:43321400-43324800 Weak transcription HSMM muscle
15 chr19:43321400-43337400 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin

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