Variant report

Variant rs16961951
Chromosome Location chr18:29034675-29034676
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr18:29030400-29048000 Weak transcription Duodenum Mucosa Duodenum
2 chr18:29033600-29035000 Enhancers NH-A brain
3 chr18:29033600-29035200 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
4 chr18:29034200-29035200 Flanking Active TSS Foreskin Keratinocyte Primary Cells skin03 Skin
5 chr18:29034200-29035600 Enhancers Hela-S3 cervix
6 chr18:29034400-29036000 Genic enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
7 chr18:29034400-29036000 Enhancers Placenta Amnion Placenta Amnion
8 chr18:29034400-29036200 Enhancers Breast Myoepithelial Primary Cells Breast
9 chr18:29034600-29035000 Flanking Active TSS Foreskin Keratinocyte Primary Cells skin02 Skin
10 chr18:29034600-29035000 Enhancers Esophagus oesophagus
11 chr18:29034600-29035000 Enhancers A549 lung
12 chr18:29034600-29035000 Enhancers NHEK skin
13 chr18:29034600-29036200 Enhancers HMEC breast

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