Variant report

Variant rs56255048
Chromosome Location chr9:97601492-97601493
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:22 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:97571800-97622600 Weak transcription Primary B cells from cord blood blood
2 chr9:97572000-97601600 Weak transcription Primary T cells fromperipheralblood blood
3 chr9:97581800-97609600 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
4 chr9:97585000-97609600 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
5 chr9:97589200-97602000 Weak transcription Lung lung
6 chr9:97589200-97605400 Weak transcription Spleen Spleen
7 chr9:97589200-97609400 Weak transcription Pancreas Pancrea
8 chr9:97589200-97622400 Weak transcription Aorta Aorta
9 chr9:97590400-97602000 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
10 chr9:97590600-97609600 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
11 chr9:97590600-97616000 Weak transcription Rectal Mucosa Donor 31 rectum
12 chr9:97591000-97609200 Weak transcription Osteobl bone
13 chr9:97592200-97608400 Weak transcription HSMMtube muscle
14 chr9:97592200-97609400 Weak transcription NHDF-Ad bronchial
15 chr9:97597200-97603000 Weak transcription Liver Liver
16 chr9:97598400-97604600 Weak transcription HepG2 liver
17 chr9:97599000-97602000 Weak transcription Stomach Mucosa stomach
18 chr9:97600000-97609400 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
19 chr9:97600200-97609600 Weak transcription Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
20 chr9:97600800-97609000 Weak transcription HSMM muscle
21 chr9:97601000-97604600 Weak transcription Primary T regulatory cells fromperipheralblood blood
22 chr9:97601400-97602200 Enhancers Primary Natural Killer cells fromperipheralblood blood

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