Variant report

Variant rs79763115
Chromosome Location chr6:106814910-106814911
allele C/T
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 chr6:106814400-106815000 Genic enhancers Breast Myoepithelial Primary Cells Breast
8 chr6:106814600-106815000 Strong transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast

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