Variant report

Variant rs11612674
Chromosome Location chr12:106617392-106617393
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr12:106606600-106626400 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
2 chr12:106614800-106621000 Weak transcription Esophagus oesophagus
3 chr12:106615000-106621200 Weak transcription Pancreatic Islets Pancreatic Islet
4 chr12:106615800-106617400 Weak transcription Adipose Nuclei Adipose
5 chr12:106616000-106617400 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
6 chr12:106617000-106617400 Enhancers Aorta Aorta
7 chr12:106617000-106618200 Enhancers Stomach Smooth Muscle stomach
8 chr12:106617000-106618600 Enhancers Ovary ovary
9 chr12:106617200-106618000 Enhancers Skeletal Muscle Male skeletal muscle
10 chr12:106617200-106618000 Enhancers Skeletal Muscle Female skeletal muscle
11 chr12:106617200-106618000 Enhancers HSMM muscle
12 chr12:106617200-106618400 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
13 chr12:106617200-106618600 Enhancers H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
14 chr12:106617200-106618600 Enhancers hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived

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