Variant report

Variant rs36070067
Chromosome Location chr19:52288408-52288409
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr19:52280800-52294000 Enhancers Primary monocytes fromperipheralblood blood
2 chr19:52286600-52289000 Enhancers K562 blood
3 chr19:52286800-52289000 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
4 chr19:52286800-52289200 Enhancers NHEK skin
5 chr19:52287400-52288600 Weak transcription HMEC breast
6 chr19:52287400-52288600 Enhancers Monocytes-CD14+_RO01746 blood
7 chr19:52287800-52288800 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
8 chr19:52287800-52289000 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
9 chr19:52287800-52289000 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
10 chr19:52287800-52292600 Weak transcription Placenta Amnion Placenta Amnion
11 chr19:52287800-52293400 Enhancers Placenta Placenta
12 chr19:52288000-52288600 Active TSS Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
13 chr19:52288400-52288600 Enhancers H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
14 chr19:52288400-52288600 Enhancers Right Atrium heart
15 chr19:52288400-52288800 Flanking Active TSS Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
16 chr19:52288400-52288800 Enhancers Fetal Heart heart
17 chr19:52288400-52289000 ZNF genes & repeats Primary B cells from peripheral blood blood
18 chr19:52288400-52289000 Flanking Active TSS Osteobl bone

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