Variant report

Variant rs12957659
Chromosome Location chr18:28811005-28811006
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:19 , 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 chr18:28809400-28811400 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
6 chr18:28809400-28811600 Enhancers NHEK skin
7 chr18:28809600-28811400 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
8 chr18:28809600-28811600 Enhancers Breast Myoepithelial Primary Cells Breast
9 chr18:28809600-28812600 Enhancers HepG2 liver
10 chr18:28809600-28813800 Enhancers Fetal Intestine Large intestine
11 chr18:28809600-28813800 Enhancers Fetal Intestine Small intestine
12 chr18:28809800-28811200 Enhancers NH-A brain
13 chr18:28809800-28813800 Enhancers Duodenum Mucosa Duodenum
14 chr18:28810600-28811400 Enhancers GM12878-XiMat blood
15 chr18:28810600-28811600 Flanking Active TSS Liver Liver
16 chr18:28810800-28811600 Enhancers HMEC breast
17 chr18:28811000-28811200 Enhancers A549 lung
18 chr18:28811000-28811400 Enhancers H1 Derived Mesenchymal Stem Cells ES cell derived
19 chr18:28811000-28811600 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin

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