Variant report

Variant rs368207438
Chromosome Location chr9:110429569-110429570
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:110413000-110437000 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
2 chr9:110426000-110435600 Weak transcription ES-I3 Cell Line embryonic stem cell
3 chr9:110427600-110429600 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
4 chr9:110427600-110429600 Weak transcription HSMMtube muscle
5 chr9:110429200-110429800 Enhancers Primary monocytes fromperipheralblood blood
6 chr9:110429200-110429800 Enhancers Monocytes-CD14+_RO01746 blood
7 chr9:110429200-110430600 Enhancers Fetal Muscle Trunk muscle
8 chr9:110429200-110430600 Enhancers Fetal Muscle Leg muscle
9 chr9:110429400-110429800 Enhancers Right Atrium heart
10 chr9:110429400-110430000 Enhancers Placenta Placenta
11 chr9:110429400-110430000 Enhancers Spleen Spleen
12 chr9:110429400-110430400 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
13 chr9:110429400-110430400 Enhancers Fetal Adrenal Gland Adrenal Gland
14 chr9:110429400-110430400 Enhancers Fetal Lung lung
15 chr9:110429400-110430400 Enhancers Fetal Stomach stomach
16 chr9:110429400-110430600 Enhancers Brain Hippocampus Middle brain
17 chr9:110429400-110430600 Enhancers Skeletal Muscle Male skeletal muscle

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