Variant report

Variant rs11792803
Chromosome Location chr9:110523789-110523790
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:20 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:110518200-110544600 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
2 chr9:110521200-110524000 Enhancers Placenta Placenta
3 chr9:110521200-110524400 Enhancers Spleen Spleen
4 chr9:110521600-110530400 Weak transcription Fetal Adrenal Gland Adrenal Gland
5 chr9:110521800-110524000 Enhancers Duodenum Mucosa Duodenum
6 chr9:110522200-110524000 Enhancers Right Atrium heart
7 chr9:110522200-110524000 Flanking Active TSS Monocytes-CD14+_RO01746 blood
8 chr9:110523000-110524000 Flanking Active TSS Primary hematopoietic stem cells G-CSF-mobilized Male --
9 chr9:110523000-110524000 Enhancers Small Intestine intestine
10 chr9:110523200-110523800 Weak transcription Stomach Mucosa stomach
11 chr9:110523200-110524000 Enhancers Skeletal Muscle Male skeletal muscle
12 chr9:110523200-110525400 Enhancers Primary monocytes fromperipheralblood blood
13 chr9:110523200-110535200 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
14 chr9:110523400-110523800 Flanking Active TSS Primary hematopoietic stem cells blood
15 chr9:110523400-110524600 Enhancers Primary hematopoietic stem cells short term culture blood
16 chr9:110523600-110524000 Enhancers Liver Liver
17 chr9:110523600-110524200 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Female --
18 chr9:110523600-110524400 Enhancers Primary neutrophils fromperipheralblood blood
19 chr9:110523600-110524600 Enhancers Adipose Nuclei Adipose
20 chr9:110523600-110528000 Weak transcription Left Ventricle heart

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