Variant report

Variant rs73204034
Chromosome Location chr12:116839021-116839022
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr12:116830200-116843800 Weak transcription NHLF lung
2 chr12:116833800-116844200 Weak transcription Osteobl bone
3 chr12:116835000-116843000 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
4 chr12:116835200-116839400 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
5 chr12:116835200-116840000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
6 chr12:116835400-116839400 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
7 chr12:116835400-116843400 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
8 chr12:116836400-116840000 Weak transcription Esophagus oesophagus
9 chr12:116836400-116843000 Weak transcription NHDF-Ad bronchial
10 chr12:116837600-116840800 ZNF genes & repeats Primary hematopoietic stem cells short term culture blood
11 chr12:116838400-116840400 ZNF genes & repeats Primary B cells from peripheral blood blood
12 chr12:116839000-116839400 Flanking Active TSS Monocytes-CD14+_RO01746 blood
13 chr12:116839000-116839800 Enhancers Dnd41 blood
14 chr12:116839000-116840000 Enhancers Fetal Muscle Leg muscle
15 chr12:116839000-116841200 ZNF genes & repeats Primary monocytes fromperipheralblood blood
16 chr12:116839000-116841200 ZNF genes & repeats Primary neutrophils fromperipheralblood blood

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