Variant report

Variant rs9805487
Chromosome Location chr13:39390861-39390862
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:12 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr13:39388800-39392600 Weak transcription Cortex derived primary cultured neurospheres brain
2 chr13:39389000-39397400 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
3 chr13:39389200-39393200 Weak transcription Pancreas Pancrea
4 chr13:39389200-39404800 Weak transcription Gastric stomach
5 chr13:39389400-39395800 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
6 chr13:39389400-39423000 Weak transcription Fetal Adrenal Gland Adrenal Gland
7 chr13:39390000-39392600 Weak transcription Ganglion Eminence derived primary cultured neurospheres brain
8 chr13:39390000-39393000 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
9 chr13:39390000-39393000 Weak transcription HMEC breast
10 chr13:39390000-39393000 Weak transcription NHEK skin
11 chr13:39390000-39395800 Weak transcription Breast Myoepithelial Primary Cells Breast
12 chr13:39390200-39393200 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast

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