Variant report

Variant rs72914749
Chromosome Location chr18:28813131-28813132
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:21 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr18:28807800-28813600 Weak transcription Stomach Mucosa stomach
2 chr18:28808200-28813200 Weak transcription Fetal Heart heart
3 chr18:28809600-28813800 Enhancers Fetal Intestine Large intestine
4 chr18:28809600-28813800 Enhancers Fetal Intestine Small intestine
5 chr18:28809800-28813800 Enhancers Duodenum Mucosa Duodenum
6 chr18:28811200-28813800 Weak transcription A549 lung
7 chr18:28811400-28813200 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
8 chr18:28811400-28813600 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
9 chr18:28811600-28813600 Weak transcription HMEC breast
10 chr18:28811600-28813600 Weak transcription NHEK skin
11 chr18:28811600-28813800 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
12 chr18:28811600-28813800 Enhancers Liver Liver
13 chr18:28811800-28813600 Enhancers GM12878-XiMat blood
14 chr18:28812000-28815000 Enhancers Breast Myoepithelial Primary Cells Breast
15 chr18:28812200-28814200 Enhancers Pancreas Pancrea
16 chr18:28812400-28813200 Enhancers Fetal Kidney kidney
17 chr18:28812600-28814200 Flanking Active TSS HepG2 liver
18 chr18:28812800-28814200 Enhancers Rectal Mucosa Donor 31 rectum
19 chr18:28813000-28813200 Enhancers H1 Derived Mesenchymal Stem Cells ES cell derived
20 chr18:28813000-28813600 Weak transcription Left Ventricle heart
21 chr18:28813000-28813800 Weak transcription Esophagus oesophagus

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