Variant report

Variant rs17005821
Chromosome Location chr3:69452827-69452828
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr3:69440000-69453800 Weak transcription HMEC breast
2 chr3:69447600-69453400 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
3 chr3:69448000-69454000 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
4 chr3:69448000-69454000 Weak transcription Brain Substantia Nigra brain
5 chr3:69448200-69454400 Weak transcription Monocytes-CD14+_RO01746 blood
6 chr3:69448600-69454400 Weak transcription Primary monocytes fromperipheralblood blood
7 chr3:69450600-69461400 Weak transcription H9 Cell Line embryonic stem cell
8 chr3:69451400-69453800 Weak transcription Fetal Brain Male brain
9 chr3:69452200-69454000 Enhancers Rectal Mucosa Donor 31 rectum
10 chr3:69452400-69453000 Enhancers Brain Hippocampus Middle brain
11 chr3:69452400-69453200 Enhancers Placenta Amnion Placenta Amnion
12 chr3:69452400-69453800 Enhancers Rectal Mucosa Donor 29 rectum
13 chr3:69452600-69453400 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
14 chr3:69452600-69453600 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
15 chr3:69452600-69453800 Weak transcription Fetal Lung lung
16 chr3:69452800-69453000 Enhancers Fetal Brain Female brain
17 chr3:69452800-69453400 Enhancers NHEK skin
18 chr3:69452800-69454000 Weak transcription Breast Myoepithelial Primary Cells Breast

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