Variant report

Variant rs10232429
Chromosome Location chr7:6885635-6885636
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:9 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr7:6883800-6893800 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
2 chr7:6885200-6885800 Enhancers H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
3 chr7:6885200-6886000 Flanking Active TSS Dnd41 blood
4 chr7:6885400-6886000 Enhancers Fetal Thymus thymus
5 chr7:6885600-6885800 Flanking Active TSS HepG2 liver
6 chr7:6885600-6886000 Bivalent Enhancer Primary T cells fromperipheralblood blood
7 chr7:6885600-6886000 Enhancers Primary hematopoietic stem cells blood
8 chr7:6885600-6886000 Flanking Active TSS Primary hematopoietic stem cells G-CSF-mobilized Male --
9 chr7:6885600-6886200 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Female --

Quick Search:


  
Input of quick search could be:

what's new

Quick links