Variant report

Variant rs2749085
Chromosome Location chr6:106811239-106811240
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 chr6:106810600-106811400 Enhancers Breast Myoepithelial Primary Cells Breast
3 chr6:106810600-106811400 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
4 chr6:106810600-106811400 Weak transcription Esophagus oesophagus
5 chr6:106810600-106811600 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
6 chr6:106810600-106817000 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
7 chr6:106810800-106816200 Weak transcription HMEC breast
8 chr6:106811200-106811400 Strong transcription NHEK skin

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