Variant report

Variant rs648192
Chromosome Location chr19:39562782-39562783
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr19:39545200-39564400 Weak transcription Brain Substantia Nigra brain
2 chr19:39557000-39564400 Weak transcription Brain Hippocampus Middle brain
3 chr19:39561800-39563800 Weak transcription Osteobl bone
4 chr19:39561800-39564000 Weak transcription Muscle Satellite Cultured Cells --
5 chr19:39562000-39563000 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
6 chr19:39562000-39563200 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
7 chr19:39562000-39563200 Weak transcription Placenta Placenta
8 chr19:39562000-39563600 Weak transcription A549 lung
9 chr19:39562000-39563800 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
10 chr19:39562000-39563800 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
11 chr19:39562000-39563800 Weak transcription NHEK skin
12 chr19:39562000-39564000 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
13 chr19:39562000-39564000 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
14 chr19:39562000-39564200 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
15 chr19:39562000-39570000 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
16 chr19:39562200-39563800 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
17 chr19:39562400-39563800 Weak transcription HMEC breast
18 chr19:39562400-39564400 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin

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