Variant report

Variant rs6720217
Chromosome Location chr2:173063489-173063490
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:173060600-173063800 Enhancers Placenta Amnion Placenta Amnion
2 chr2:173060600-173064400 Enhancers Primary monocytes fromperipheralblood blood
3 chr2:173060600-173064400 Enhancers Fetal Thymus thymus
4 chr2:173061600-173064400 Enhancers HMEC breast
5 chr2:173062000-173065200 Enhancers Primary neutrophils fromperipheralblood blood
6 chr2:173062200-173063600 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Male --
7 chr2:173062200-173063800 Enhancers Monocytes-CD14+_RO01746 blood
8 chr2:173062200-173064400 Enhancers Breast Myoepithelial Primary Cells Breast
9 chr2:173062200-173064400 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
10 chr2:173062200-173064800 Weak transcription Primary hematopoietic stem cells blood
11 chr2:173062400-173064200 Enhancers NHEK skin
12 chr2:173062600-173063800 Enhancers H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
13 chr2:173062600-173064400 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
14 chr2:173063200-173063800 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
15 chr2:173063400-173063800 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Female --

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