Variant report

Variant rs72994874
Chromosome Location chr2:133714929-133714930
allele A/T
Outlinks Ensembl   UCSC
Chromatin state (count:12 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:133699200-133720600 Weak transcription Fetal Lung lung
2 chr2:133701600-133727000 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
3 chr2:133702200-133724400 Weak transcription Brain Hippocampus Middle brain
4 chr2:133705600-133720600 Weak transcription Fetal Stomach stomach
5 chr2:133709600-133721600 Weak transcription Ganglion Eminence derived primary cultured neurospheres brain
6 chr2:133709800-133720600 Weak transcription Fetal Kidney kidney
7 chr2:133709800-133721600 Weak transcription Cortex derived primary cultured neurospheres brain
8 chr2:133710400-133719800 Weak transcription H9 Derived Neuron Cultured Cells ES cell derived
9 chr2:133711600-133716800 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
10 chr2:133713600-133722400 Strong transcription H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
11 chr2:133714400-133718600 Weak transcription Pancreas Pancrea
12 chr2:133714600-133735400 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast

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