Variant report

Variant rs12981538
Chromosome Location chr19:52289962-52289963
allele A/T
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr19:52280800-52294000 Enhancers Primary monocytes fromperipheralblood blood
2 chr19:52287800-52292600 Weak transcription Placenta Amnion Placenta Amnion
3 chr19:52287800-52293400 Enhancers Placenta Placenta
4 chr19:52288600-52292600 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
5 chr19:52288600-52300800 Weak transcription Right Atrium heart
6 chr19:52288800-52290000 Weak transcription Fetal Heart heart
7 chr19:52289000-52290000 Weak transcription Primary B cells from peripheral blood blood
8 chr19:52289000-52290000 Weak transcription K562 blood
9 chr19:52289000-52292200 Weak transcription Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
10 chr19:52289000-52292400 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
11 chr19:52289000-52292400 Weak transcription Osteobl bone
12 chr19:52289200-52292400 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
13 chr19:52289800-52290400 Flanking Active TSS Monocytes-CD14+_RO01746 blood

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