Variant report

Variant rs55780983
Chromosome Location chr19:43493025-43493026
allele A/C
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr19:43490800-43494600 Enhancers NHEK skin
2 chr19:43492200-43493200 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
3 chr19:43492200-43493200 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
4 chr19:43492200-43493200 Weak transcription NHLF lung
5 chr19:43492200-43493400 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
6 chr19:43492200-43493400 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
7 chr19:43492200-43495200 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
8 chr19:43492400-43493200 Weak transcription Osteobl bone
9 chr19:43492400-43493400 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
10 chr19:43492400-43493400 Weak transcription Muscle Satellite Cultured Cells --
11 chr19:43492400-43495800 Weak transcription Placenta Placenta
12 chr19:43492400-43496200 Weak transcription Breast Myoepithelial Primary Cells Breast
13 chr19:43493000-43493800 Enhancers NHDF-Ad bronchial
14 chr19:43493000-43494400 Enhancers HMEC breast

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