Variant report

Variant rs10191165
Chromosome Location chr2:173062261-173062262
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:173060400-173062400 Enhancers Stomach Mucosa stomach
2 chr2:173060600-173063800 Enhancers Placenta Amnion Placenta Amnion
3 chr2:173060600-173064400 Enhancers Primary monocytes fromperipheralblood blood
4 chr2:173060600-173064400 Enhancers Fetal Thymus thymus
5 chr2:173061000-173062400 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Female --
6 chr2:173061400-173062600 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
7 chr2:173061600-173064400 Enhancers HMEC breast
8 chr2:173061800-173062600 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
9 chr2:173061800-173063200 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
10 chr2:173062000-173062400 Flanking Active TSS NHEK skin
11 chr2:173062000-173063400 Enhancers Duodenum Mucosa Duodenum
12 chr2:173062000-173065200 Enhancers Primary neutrophils fromperipheralblood blood
13 chr2:173062200-173063600 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Male --
14 chr2:173062200-173063800 Enhancers Monocytes-CD14+_RO01746 blood
15 chr2:173062200-173064400 Enhancers Breast Myoepithelial Primary Cells Breast
16 chr2:173062200-173064400 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
17 chr2:173062200-173064800 Weak transcription Primary hematopoietic stem cells blood

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