Variant report

Variant rs11634999
Chromosome Location chr15:51871461-51871462
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:11 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr15:51867800-51872400 Enhancers K562 blood
2 chr15:51868600-51872000 Flanking Active TSS Monocytes-CD14+_RO01746 blood
3 chr15:51869000-51871600 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
4 chr15:51869600-51875200 Enhancers Primary neutrophils fromperipheralblood blood
5 chr15:51869600-51889600 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
6 chr15:51870000-51875200 Enhancers Primary monocytes fromperipheralblood blood
7 chr15:51870400-51871600 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
8 chr15:51870800-51882400 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
9 chr15:51871200-51871600 Enhancers Adipose Nuclei Adipose
10 chr15:51871200-51871800 Enhancers Primary hematopoietic stem cells short term culture blood
11 chr15:51871400-51871600 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell

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