Variant report

Variant rs28506968
Chromosome Location chr20:53171074-53171075
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:12 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr20:53162200-53172600 Weak transcription Skeletal Muscle Female skeletal muscle
2 chr20:53162400-53171600 Weak transcription iPS-15b Cell Line embryonic stem cell
3 chr20:53166400-53177400 Weak transcription Ganglion Eminence derived primary cultured neurospheres brain
4 chr20:53166800-53173600 Weak transcription Cortex derived primary cultured neurospheres brain
5 chr20:53166800-53176800 Weak transcription Breast Myoepithelial Primary Cells Breast
6 chr20:53167800-53174000 Weak transcription Osteobl bone
7 chr20:53167800-53189200 Weak transcription Aorta Aorta
8 chr20:53170800-53171600 Enhancers iPS-20b Cell Line embryonic stem cell
9 chr20:53170800-53172000 Enhancers H1 Cell Line embryonic stem cell
10 chr20:53171000-53171200 Enhancers H9 Cell Line embryonic stem cell
11 chr20:53171000-53171400 Enhancers Fetal Brain Female brain
12 chr20:53171000-53171800 Enhancers iPS-18 Cell Line embryonic stem cell

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