Variant report

Variant rs369304491
Chromosome Location chr6:106814054-106814055
allele -/G
Outlinks Ensembl   UCSC
Chromatin state (count:8 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:106810400-106817200 Weak transcription Fetal Intestine Large intestine
2 chr6:106810600-106817000 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
3 chr6:106810800-106816200 Weak transcription HMEC breast
4 chr6:106811600-106816000 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
5 chr6:106812000-106816400 Weak transcription NHEK skin
6 chr6:106812200-106818000 Weak transcription Esophagus oesophagus
7 chr6:106813600-106814200 Enhancers Breast Myoepithelial Primary Cells Breast
8 chr6:106813800-106814400 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast

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