Variant report

Variant rs12604279
Chromosome Location chr18:29048540-29048541
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:10 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr18:29036000-29064600 Weak transcription Placenta Amnion Placenta Amnion
2 chr18:29036600-29061200 Strong transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
3 chr18:29036800-29059600 Strong transcription Foreskin Keratinocyte Primary Cells skin02 Skin
4 chr18:29036800-29060400 Strong transcription Foreskin Keratinocyte Primary Cells skin03 Skin
5 chr18:29036800-29060400 Strong transcription NHEK skin
6 chr18:29036800-29062400 Strong transcription HMEC breast
7 chr18:29043400-29050800 Weak transcription Fetal Heart heart
8 chr18:29046200-29049200 Strong transcription Esophagus oesophagus
9 chr18:29047800-29049800 Strong transcription Breast Myoepithelial Primary Cells Breast
10 chr18:29048000-29049600 Strong transcription Duodenum Mucosa Duodenum

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