Variant report

Variant rs12190136
Chromosome Location chr6:44767072-44767073
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:44761800-44776200 Weak transcription ES-I3 Cell Line embryonic stem cell
2 chr6:44762000-44768000 Weak transcription Ganglion Eminence derived primary cultured neurospheres brain
3 chr6:44765000-44767200 Enhancers Primary monocytes fromperipheralblood blood
4 chr6:44765200-44768800 Weak transcription HUES6 Cell Line embryonic stem cell
5 chr6:44766000-44768000 Weak transcription H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
6 chr6:44766200-44768000 Weak transcription H9 Derived Neuron Cultured Cells ES cell derived
7 chr6:44766200-44768000 Weak transcription hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
8 chr6:44766400-44767200 Enhancers Colon Smooth Muscle Colon
9 chr6:44766800-44768000 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
10 chr6:44767000-44767200 Enhancers iPS-18 Cell Line embryonic stem cell
11 chr6:44767000-44767200 Enhancers Fetal Kidney kidney
12 chr6:44767000-44767200 Enhancers Lung lung
13 chr6:44767000-44767200 Enhancers Pancreas Pancrea
14 chr6:44767000-44767600 Bivalent Enhancer HepG2 liver
15 chr6:44767000-44769200 Enhancers Fetal Intestine Large intestine

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