Variant report

Variant rs4078622
Chromosome Location chr19:43386156-43386157
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:12 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr19:43381600-43386200 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
2 chr19:43381600-43386200 Weak transcription NHEK skin
3 chr19:43381600-43387000 Weak transcription Muscle Satellite Cultured Cells --
4 chr19:43382200-43389000 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
5 chr19:43384000-43389000 Weak transcription NHDF-Ad bronchial
6 chr19:43384400-43386200 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
7 chr19:43384400-43388400 Weak transcription Breast Myoepithelial Primary Cells Breast
8 chr19:43384400-43389000 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
9 chr19:43385600-43387600 Enhancers HMEC breast
10 chr19:43385600-43388600 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
11 chr19:43385600-43388600 Weak transcription Placenta Placenta
12 chr19:43386000-43386400 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast

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