Variant report

Variant rs16932442
Chromosome Location chr9:118022616-118022617
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:12 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:118014000-118023400 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
2 chr9:118014200-118023000 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
3 chr9:118014400-118023800 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
4 chr9:118015600-118023400 Weak transcription Fetal Muscle Trunk muscle
5 chr9:118016000-118023600 Weak transcription H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
6 chr9:118017400-118023600 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
7 chr9:118017600-118023200 Weak transcription Fetal Muscle Leg muscle
8 chr9:118018000-118023400 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
9 chr9:118018000-118023600 Weak transcription Colon Smooth Muscle Colon
10 chr9:118018200-118024000 Weak transcription Fetal Lung lung
11 chr9:118018200-118024000 Weak transcription Rectal Smooth Muscle rectum
12 chr9:118020200-118023000 Weak transcription NHEK skin

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