Variant report

Variant rs9921281
Chromosome Location chr16:72366703-72366704
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr16:72354200-72366800 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
2 chr16:72354200-72366800 Weak transcription Pancreas Pancrea
3 chr16:72354200-72368400 Weak transcription HepG2 liver
4 chr16:72354200-72368600 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
5 chr16:72355600-72366800 Weak transcription Primary B cells from cord blood blood
6 chr16:72358800-72366800 Weak transcription Thymus Thymus
7 chr16:72358800-72366800 Weak transcription Dnd41 blood
8 chr16:72362200-72368200 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
9 chr16:72363400-72366800 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
10 chr16:72365600-72368200 Weak transcription H9 Cell Line embryonic stem cell
11 chr16:72366000-72366800 Weak transcription hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
12 chr16:72366000-72367400 ZNF genes & repeats Primary hematopoietic stem cells G-CSF-mobilized Male --
13 chr16:72366600-72367000 ZNF genes & repeats Monocytes-CD14+_RO01746 blood

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