Variant report

Variant rs13055063
Chromosome Location chr22:33513026-33513027
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr22:33511400-33513200 Weak transcription Placenta Amnion Placenta Amnion
2 chr22:33512000-33513400 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
3 chr22:33512200-33515200 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
4 chr22:33512600-33513400 Enhancers HUES6 Cell Line embryonic stem cell
5 chr22:33512600-33513400 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Female --
6 chr22:33512600-33513600 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Male --
7 chr22:33512600-33514000 Enhancers Primary hematopoietic stem cells short term culture blood
8 chr22:33512600-33514800 Enhancers HMEC breast
9 chr22:33512600-33515200 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
10 chr22:33512800-33513200 Flanking Active TSS ES-I3 Cell Line embryonic stem cell
11 chr22:33512800-33513400 Enhancers hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
12 chr22:33512800-33513400 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
13 chr22:33512800-33513800 Enhancers Primary hematopoietic stem cells blood
14 chr22:33513000-33513200 Enhancers NHEK skin
15 chr22:33513000-33513400 Enhancers ES-WA7 Cell Line embryonic stem cell

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