Variant report

Variant rs66889852
Chromosome Location chr18:29036842-29036843
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:10 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr18:29030400-29048000 Weak transcription Duodenum Mucosa Duodenum
2 chr18:29035000-29038600 Weak transcription Esophagus oesophagus
3 chr18:29036000-29064600 Weak transcription Placenta Amnion Placenta Amnion
4 chr18:29036200-29038600 Weak transcription Breast Myoepithelial Primary Cells Breast
5 chr18:29036600-29061200 Strong transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
6 chr18:29036800-29037200 Enhancers iPS-20b Cell Line embryonic stem cell
7 chr18:29036800-29059600 Strong transcription Foreskin Keratinocyte Primary Cells skin02 Skin
8 chr18:29036800-29060400 Strong transcription Foreskin Keratinocyte Primary Cells skin03 Skin
9 chr18:29036800-29060400 Strong transcription NHEK skin
10 chr18:29036800-29062400 Strong transcription HMEC breast

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