Variant report

Variant rs73661347
Chromosome Location chr8:6950341-6950342
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr8:6949400-6950400 Bivalent/Poised TSS HUES6 Cell Line embryonic stem cell
2 chr8:6949400-6950400 Bivalent/Poised TSS iPS-15b Cell Line embryonic stem cell
3 chr8:6949600-6950400 Bivalent/Poised TSS iPS-18 Cell Line embryonic stem cell
4 chr8:6949600-6950400 Enhancers Primary T helper memory cells from peripheral blood 1 blood
5 chr8:6949600-6950600 Active TSS Breast Myoepithelial Primary Cells Breast
6 chr8:6949800-6950400 Bivalent Enhancer H1 Derived Mesenchymal Stem Cells ES cell derived
7 chr8:6949800-6950400 Bivalent Enhancer Fetal Muscle Trunk muscle
8 chr8:6950000-6950400 Flanking Bivalent TSS/Enh HUES48 Cell Line embryonic stem cell
9 chr8:6950000-6950800 Flanking Active TSS Dnd41 blood
10 chr8:6950200-6950400 Flanking Bivalent TSS/Enh iPS DF 19.11 Cell Line embryonic stem cell
11 chr8:6950200-6950400 Enhancers Primary B cells from peripheral blood blood
12 chr8:6950200-6950400 Bivalent Enhancer Ganglion Eminence derived primary cultured neurospheres brain
13 chr8:6950200-6950600 Bivalent Enhancer H1 Cell Line embryonic stem cell
14 chr8:6950200-6950600 Enhancers Primary neutrophils fromperipheralblood blood

Quick Search:


  
Input of quick search could be:

what's new

Quick links