Variant report

Variant rs536814879
Chromosome Location chr8:9642196-9642197
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr8:9638600-9644800 Weak transcription HSMM muscle
2 chr8:9638600-9645400 Weak transcription Fetal Brain Male brain
3 chr8:9640000-9642200 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
4 chr8:9640400-9646800 Weak transcription Pancreas Pancrea
5 chr8:9641000-9642600 ZNF genes & repeats hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
6 chr8:9641600-9642200 Enhancers HMEC breast
7 chr8:9641600-9642400 ZNF genes & repeats ES-UCSF4 Cell Line embryonic stem cell
8 chr8:9641800-9643600 Weak transcription Fetal Heart heart
9 chr8:9642000-9642200 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
10 chr8:9642000-9642200 Active TSS Primary T cells from cord blood blood
11 chr8:9642000-9642600 ZNF genes & repeats Pancreatic Islets Pancreatic Islet
12 chr8:9642000-9642800 ZNF genes & repeats ES-I3 Cell Line embryonic stem cell
13 chr8:9642000-9642800 ZNF genes & repeats Ganglion Eminence derived primary cultured neurospheres brain

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