Variant report

Variant rs7860628
Chromosome Location chr9:95538914-95538915
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:10 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:95533200-95541200 Weak transcription Left Ventricle heart
2 chr9:95533400-95541200 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
3 chr9:95533400-95543200 Weak transcription Esophagus oesophagus
4 chr9:95536600-95539000 Enhancers Primary monocytes fromperipheralblood blood
5 chr9:95537200-95543800 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
6 chr9:95537600-95544000 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
7 chr9:95538200-95539000 Enhancers Monocytes-CD14+_RO01746 blood
8 chr9:95538200-95543800 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
9 chr9:95538400-95541000 Weak transcription Primary B cells from cord blood blood
10 chr9:95538800-95543600 Enhancers Primary neutrophils fromperipheralblood blood

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