Variant report

Variant rs34187983
Chromosome Location chr18:28811486-28811487
allele C/G
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 chr18:28809400-28811600 Enhancers NHEK skin
6 chr18:28809600-28811600 Enhancers Breast Myoepithelial Primary Cells Breast
7 chr18:28809600-28812600 Enhancers HepG2 liver
8 chr18:28809600-28813800 Enhancers Fetal Intestine Large intestine
9 chr18:28809600-28813800 Enhancers Fetal Intestine Small intestine
10 chr18:28809800-28813800 Enhancers Duodenum Mucosa Duodenum
11 chr18:28810600-28811600 Flanking Active TSS Liver Liver
12 chr18:28810800-28811600 Enhancers HMEC breast
13 chr18:28811000-28811600 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
14 chr18:28811200-28813800 Weak transcription A549 lung
15 chr18:28811400-28811800 Flanking Active TSS GM12878-XiMat blood
16 chr18:28811400-28813000 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
17 chr18:28811400-28813200 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
18 chr18:28811400-28813600 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin

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