Variant report

Variant rs67014182
Chromosome Location chr18:28811801-28811802
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr18:28806200-28812200 Weak transcription Pancreas Pancrea
2 chr18:28807400-28812400 Weak transcription Left Ventricle heart
3 chr18:28807800-28813600 Weak transcription Stomach Mucosa stomach
4 chr18:28808200-28813200 Weak transcription Fetal Heart heart
5 chr18:28809600-28812600 Enhancers HepG2 liver
6 chr18:28809600-28813800 Enhancers Fetal Intestine Large intestine
7 chr18:28809600-28813800 Enhancers Fetal Intestine Small intestine
8 chr18:28809800-28813800 Enhancers Duodenum Mucosa Duodenum
9 chr18:28811200-28813800 Weak transcription A549 lung
10 chr18:28811400-28813000 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
11 chr18:28811400-28813200 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
12 chr18:28811400-28813600 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
13 chr18:28811600-28812000 Weak transcription Breast Myoepithelial Primary Cells Breast
14 chr18:28811600-28813600 Weak transcription HMEC breast
15 chr18:28811600-28813600 Weak transcription NHEK skin
16 chr18:28811600-28813800 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
17 chr18:28811600-28813800 Enhancers Liver Liver
18 chr18:28811800-28813600 Enhancers GM12878-XiMat blood

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