Variant report

Variant rs72756468
Chromosome Location chr9:95443565-95443566
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:11 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:95433800-95444000 Weak transcription Fetal Brain Female brain
2 chr9:95441800-95444200 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
3 chr9:95441800-95444400 Enhancers HMEC breast
4 chr9:95442200-95443600 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
5 chr9:95442400-95443600 Flanking Active TSS NHEK skin
6 chr9:95443000-95443600 Weak transcription Spleen Spleen
7 chr9:95443200-95443600 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
8 chr9:95443200-95444200 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
9 chr9:95443200-95450600 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
10 chr9:95443400-95443800 Weak transcription Esophagus oesophagus
11 chr9:95443400-95444200 Flanking Active TSS Foreskin Keratinocyte Primary Cells skin02 Skin

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