Variant report

Variant rs17795913
Chromosome Location chr9:102178789-102178790
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:102177600-102179000 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
2 chr9:102177800-102178800 Enhancers Primary hematopoietic stem cells short term culture blood
3 chr9:102177800-102178800 Enhancers GM12878-XiMat blood
4 chr9:102177800-102179600 Enhancers Foreskin Fibroblast Primary Cells skin02 Skin
5 chr9:102178000-102178800 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Male --
6 chr9:102178000-102178800 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
7 chr9:102178000-102178800 Enhancers NHEK skin
8 chr9:102178000-102179000 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
9 chr9:102178000-102179000 Enhancers HUVEC blood vessel
10 chr9:102178000-102179000 Enhancers NHDF-Ad bronchial
11 chr9:102178200-102178800 Enhancers Monocytes-CD14+_RO01746 blood
12 chr9:102178400-102178800 Enhancers IMR90 fetal lung fibroblasts Cell Line lung
13 chr9:102178400-102178800 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Female --
14 chr9:102178400-102178800 Enhancers Fetal Brain Male brain
15 chr9:102178400-102179000 Enhancers Primary monocytes fromperipheralblood blood
16 chr9:102178600-102178800 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
17 chr9:102178600-102181200 Weak transcription Fetal Brain Female brain

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