Variant report

Variant rs2199184
Chromosome Location chr4:118715022-118715023
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:10 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr4:118712200-118719800 Weak transcription HUES48 Cell Line embryonic stem cell
2 chr4:118714600-118715600 Enhancers Fetal Lung lung
3 chr4:118714600-118715800 Enhancers Dnd41 blood
4 chr4:118714600-118715800 Enhancers NHEK skin
5 chr4:118714600-118716400 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
6 chr4:118714800-118715600 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
7 chr4:118714800-118715800 Enhancers Breast Myoepithelial Primary Cells Breast
8 chr4:118714800-118716000 Enhancers HMEC breast
9 chr4:118714800-118716400 Enhancers Stomach Mucosa stomach
10 chr4:118715000-118715600 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast

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