Variant report

Variant rs566121552
Chromosome Location chr18:29033226-29033227
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:9 , 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 chr18:29031600-29034000 Enhancers Breast Myoepithelial Primary Cells Breast
4 chr18:29032000-29034400 Weak transcription Placenta Amnion Placenta Amnion
5 chr18:29032200-29033400 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
6 chr18:29032200-29033800 Enhancers HMEC breast
7 chr18:29033200-29033400 Flanking Active TSS Foreskin Keratinocyte Primary Cells skin03 Skin
8 chr18:29033200-29033400 Flanking Active TSS NHEK skin
9 chr18:29033200-29034600 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin

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