Variant report

Variant rs9634039
Chromosome Location chr11:50761263-50761264
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr11:50730800-50770200 ZNF genes & repeats HUES48 Cell Line embryonic stem cell
2 chr11:50741200-50772800 ZNF genes & repeats hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
3 chr11:50746000-50769600 ZNF genes & repeats iPS-18 Cell Line embryonic stem cell
4 chr11:50750000-50765800 ZNF genes & repeats iPS-20b Cell Line embryonic stem cell
5 chr11:50752800-50771800 ZNF genes & repeats HUES64 Cell Line embryonic stem cell
6 chr11:50755800-50761800 Weak transcription Aorta Aorta
7 chr11:50757800-50763200 ZNF genes & repeats HUES6 Cell Line embryonic stem cell
8 chr11:50758800-50763800 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
9 chr11:50759000-50767800 Weak transcription Right Ventricle heart
10 chr11:50760000-50761800 Weak transcription Primary T killer memory cells from peripheral blood blood
11 chr11:50760000-50763000 ZNF genes & repeats Primary hematopoietic stem cells blood
12 chr11:50760200-50764800 Weak transcription K562 blood
13 chr11:50760400-50764800 Weak transcription NHLF lung
14 chr11:50761200-50763600 ZNF genes & repeats ES-I3 Cell Line embryonic stem cell

Quick Search:


  
Input of quick search could be:

what's new

Quick links