Variant report

Variant rs17761759
Chromosome Location chr19:52290034-52290035
allele A/G
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 chr19:52289000-52292200 Weak transcription Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
7 chr19:52289000-52292400 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
8 chr19:52289000-52292400 Weak transcription Osteobl bone
9 chr19:52289200-52292400 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
10 chr19:52289800-52290400 Flanking Active TSS Monocytes-CD14+_RO01746 blood
11 chr19:52290000-52290400 Enhancers Primary B cells from peripheral blood blood
12 chr19:52290000-52290800 Enhancers Fetal Heart heart
13 chr19:52290000-52291400 Enhancers K562 blood

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