Variant report

Variant rs561562736
Chromosome Location chr17:20806211-20806212
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr17:20798200-20811600 Weak transcription H9 Cell Line embryonic stem cell
2 chr17:20798800-20806800 Strong transcription H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
3 chr17:20800200-20811000 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
4 chr17:20801800-20812200 Weak transcription H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
5 chr17:20802200-20807600 Strong transcription H9 Derived Neuron Cultured Cells ES cell derived
6 chr17:20803200-20811400 Weak transcription ES-I3 Cell Line embryonic stem cell
7 chr17:20803400-20811200 Weak transcription H1 Cell Line embryonic stem cell
8 chr17:20803400-20811400 Weak transcription iPS-18 Cell Line embryonic stem cell
9 chr17:20804200-20811800 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
10 chr17:20806200-20806400 Bivalent Enhancer Primary hematopoietic stem cells G-CSF-mobilized Male --
11 chr17:20806200-20806800 Enhancers hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
12 chr17:20806200-20811000 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
13 chr17:20806200-20811400 Weak transcription HUES6 Cell Line embryonic stem cell

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