Variant report

Variant rs3106594
Chromosome Location chr13:61659844-61659845
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr13:61654600-61663800 Weak transcription H9 Cell Line embryonic stem cell
2 chr13:61655200-61662000 Weak transcription H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
3 chr13:61657000-61661000 ZNF genes & repeats hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
4 chr13:61658200-61660800 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
5 chr13:61658200-61661000 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
6 chr13:61658600-61660800 Enhancers NHEK skin
7 chr13:61659200-61660200 Enhancers HUES64 Cell Line embryonic stem cell
8 chr13:61659600-61660400 Weak transcription HUES48 Cell Line embryonic stem cell
9 chr13:61659600-61660600 Enhancers ES-I3 Cell Line embryonic stem cell
10 chr13:61659800-61660200 Enhancers iPS-20b Cell Line embryonic stem cell
11 chr13:61659800-61660600 Enhancers H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
12 chr13:61659800-61660600 Enhancers Placenta Amnion Placenta Amnion
13 chr13:61659800-61668600 Weak transcription iPS-18 Cell Line embryonic stem cell

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