Variant report

Variant rs10993257
Chromosome Location chr9:92725660-92725661
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:92723400-92725800 Enhancers Spleen Spleen
2 chr9:92723600-92726000 Flanking Active TSS Monocytes-CD14+_RO01746 blood
3 chr9:92723600-92727800 Enhancers Primary monocytes fromperipheralblood blood
4 chr9:92724000-92727400 Enhancers Primary neutrophils fromperipheralblood blood
5 chr9:92724200-92725800 Enhancers Primary B cells from cord blood blood
6 chr9:92724400-92727000 Weak transcription Right Atrium heart
7 chr9:92724800-92726200 Weak transcription Liver Liver
8 chr9:92724800-92729800 Weak transcription Fetal Adrenal Gland Adrenal Gland
9 chr9:92724800-92732400 Weak transcription Sigmoid Colon Sigmoid Colon
10 chr9:92725000-92726000 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
11 chr9:92725000-92726800 Weak transcription NHDF-Ad bronchial
12 chr9:92725000-92727600 Weak transcription Colon Smooth Muscle Colon
13 chr9:92725000-92729600 Weak transcription Fetal Intestine Small intestine
14 chr9:92725200-92726800 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
15 chr9:92725400-92731000 Weak transcription Skeletal Muscle Female skeletal muscle
16 chr9:92725600-92738200 Weak transcription Lung lung

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