Variant report

Variant rs7906119
Chromosome Location chr10:44728447-44728448
allele A/G/T
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr10:44723000-44729800 Weak transcription H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
2 chr10:44727400-44728600 Enhancers iPS-18 Cell Line embryonic stem cell
3 chr10:44727600-44728800 Enhancers HUES64 Cell Line embryonic stem cell
4 chr10:44727600-44728800 Enhancers iPS-15b Cell Line embryonic stem cell
5 chr10:44727600-44729000 Enhancers HUES48 Cell Line embryonic stem cell
6 chr10:44728000-44728800 Enhancers HUES6 Cell Line embryonic stem cell
7 chr10:44728000-44730200 Enhancers H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
8 chr10:44728000-44734200 Enhancers Placenta Placenta
9 chr10:44728200-44728800 Enhancers ES-I3 Cell Line embryonic stem cell
10 chr10:44728200-44730200 Enhancers hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
11 chr10:44728200-44731400 Enhancers ES-UCSF4 Cell Line embryonic stem cell
12 chr10:44728400-44728600 Enhancers hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
13 chr10:44728400-44729000 Flanking Active TSS iPS-20b Cell Line embryonic stem cell
14 chr10:44728400-44730600 Enhancers Fetal Stomach stomach
15 chr10:44728400-44734800 Enhancers HepG2 liver

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