Variant report

Variant rs12965829
Chromosome Location chr18:28809685-28809686
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:21 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr18:28805000-28811000 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
2 chr18:28806000-28810400 Weak transcription Hela-S3 cervix
3 chr18:28806200-28809800 Weak transcription A549 lung
4 chr18:28806200-28812200 Weak transcription Pancreas Pancrea
5 chr18:28806400-28809800 Weak transcription NH-A brain
6 chr18:28806600-28809800 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
7 chr18:28807400-28812400 Weak transcription Left Ventricle heart
8 chr18:28807800-28813600 Weak transcription Stomach Mucosa stomach
9 chr18:28808200-28813200 Weak transcription Fetal Heart heart
10 chr18:28808600-28809800 Weak transcription Duodenum Mucosa Duodenum
11 chr18:28809000-28810000 Flanking Active TSS Liver Liver
12 chr18:28809000-28810400 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
13 chr18:28809200-28810400 Enhancers HMEC breast
14 chr18:28809400-28811400 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
15 chr18:28809400-28811600 Enhancers NHEK skin
16 chr18:28809600-28810600 Flanking Active TSS GM12878-XiMat blood
17 chr18:28809600-28811400 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
18 chr18:28809600-28811600 Enhancers Breast Myoepithelial Primary Cells Breast
19 chr18:28809600-28812600 Enhancers HepG2 liver
20 chr18:28809600-28813800 Enhancers Fetal Intestine Large intestine
21 chr18:28809600-28813800 Enhancers Fetal Intestine Small intestine

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