Variant report

Variant rs9792412
Chromosome Location chr9:16025889-16025890
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:16018200-16028600 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
2 chr9:16022600-16031800 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
3 chr9:16023000-16026200 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
4 chr9:16023600-16040600 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
5 chr9:16024200-16026000 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
6 chr9:16024200-16027000 Weak transcription Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
7 chr9:16024200-16028200 Weak transcription NHLF lung
8 chr9:16024200-16028600 Weak transcription HMEC breast
9 chr9:16024600-16027000 Weak transcription NH-A brain
10 chr9:16024800-16026000 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
11 chr9:16024800-16026000 Weak transcription Osteobl bone
12 chr9:16024800-16026400 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
13 chr9:16024800-16027000 Weak transcription Muscle Satellite Cultured Cells --
14 chr9:16024800-16027000 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
15 chr9:16024800-16027800 Weak transcription NHDF-Ad bronchial
16 chr9:16025400-16026200 Enhancers Adipose Nuclei Adipose
17 chr9:16025800-16026200 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell

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