Variant report

Variant rs17658536
Chromosome Location chr18:28848593-28848594
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr18:28842400-28849000 Weak transcription HepG2 liver
2 chr18:28842600-28849200 Weak transcription Fetal Kidney kidney
3 chr18:28845800-28848800 Weak transcription Liver Liver
4 chr18:28847600-28850400 Enhancers Fetal Intestine Small intestine
5 chr18:28847800-28849200 Enhancers Stomach Mucosa stomach
6 chr18:28847800-28849600 Enhancers Breast Myoepithelial Primary Cells Breast
7 chr18:28847800-28850800 Enhancers Fetal Intestine Large intestine
8 chr18:28848000-28849400 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
9 chr18:28848000-28849400 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
10 chr18:28848000-28849800 Enhancers NHEK skin
11 chr18:28848200-28848800 Enhancers GM12878-XiMat blood
12 chr18:28848200-28849400 Enhancers HMEC breast
13 chr18:28848200-28849600 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
14 chr18:28848200-28854800 Weak transcription iPS-18 Cell Line embryonic stem cell

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