Variant report

Variant rs73230336
Chromosome Location chr12:121029618-121029619
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:12 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr12:121028000-121033200 Weak transcription Skeletal Muscle Male skeletal muscle
2 chr12:121028800-121030000 Enhancers HepG2 liver
3 chr12:121028800-121030200 Enhancers iPS DF 19.11 Cell Line embryonic stem cell
4 chr12:121029000-121029800 Enhancers Rectal Mucosa Donor 31 rectum
5 chr12:121029600-121029800 Bivalent Enhancer Foreskin Melanocyte Primary Cells skin01 Skin
6 chr12:121029600-121029800 Enhancers Brain Dorsolateral Prefrontal Cortex brain
7 chr12:121029600-121029800 Enhancers Colonic Mucosa Colon
8 chr12:121029600-121030000 Enhancers ES-I3 Cell Line embryonic stem cell
9 chr12:121029600-121030000 Bivalent Enhancer Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
10 chr12:121029600-121030200 Enhancers Primary neutrophils fromperipheralblood blood
11 chr12:121029600-121030200 Enhancers Adipose Nuclei Adipose
12 chr12:121029600-121030400 Enhancers Monocytes-CD14+_RO01746 blood

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