Variant report

Variant rs556098147
Chromosome Location chr18:29034182-29034183
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:12 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr18:29030400-29048000 Weak transcription Duodenum Mucosa Duodenum
2 chr18:29030600-29034600 Weak transcription Esophagus oesophagus
3 chr18:29032000-29034400 Weak transcription Placenta Amnion Placenta Amnion
4 chr18:29033200-29034600 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
5 chr18:29033400-29034200 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
6 chr18:29033400-29034400 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
7 chr18:29033600-29035000 Enhancers NH-A brain
8 chr18:29033600-29035200 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
9 chr18:29033800-29034200 Enhancers NHEK skin
10 chr18:29033800-29034400 Active TSS HMEC breast
11 chr18:29034000-29034200 Enhancers A549 lung
12 chr18:29034000-29034400 Weak transcription Breast Myoepithelial Primary Cells Breast

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