Variant report

Variant rs7249066
Chromosome Location chr19:43323314-43323315
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr19:43321400-43323600 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
2 chr19:43321400-43323600 Weak transcription Muscle Satellite Cultured Cells --
3 chr19:43321400-43324000 Weak transcription Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
4 chr19:43321400-43324200 Weak transcription Cortex derived primary cultured neurospheres brain
5 chr19:43321400-43324800 Weak transcription HSMM muscle
6 chr19:43321400-43337400 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
7 chr19:43321800-43323400 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
8 chr19:43321800-43323800 Weak transcription NH-A brain
9 chr19:43321800-43324000 Weak transcription Osteobl bone
10 chr19:43322800-43324200 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
11 chr19:43323000-43323400 Genic enhancers NHEK skin
12 chr19:43323000-43324400 Enhancers HMEC breast
13 chr19:43323000-43325200 Enhancers Breast Myoepithelial Primary Cells Breast
14 chr19:43323000-43325200 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
15 chr19:43323000-43325400 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
16 chr19:43323000-43326000 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
17 chr19:43323000-43326200 Enhancers NHDF-Ad bronchial
18 chr19:43323200-43325200 Enhancers NHLF lung

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