Variant report

Variant rs200149127
Chromosome Location chr12:123187749-123187750
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:23 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr12:123166600-123187800 Weak transcription A549 lung
2 chr12:123174000-123199800 Weak transcription Breast Myoepithelial Primary Cells Breast
3 chr12:123184000-123188800 Enhancers Primary monocytes fromperipheralblood blood
4 chr12:123185400-123188200 Active TSS Primary B cells from cord blood blood
5 chr12:123186000-123188000 Enhancers H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
6 chr12:123186000-123188000 Enhancers Placenta Placenta
7 chr12:123186000-123188200 Enhancers NHEK skin
8 chr12:123186000-123188600 Flanking Active TSS Primary neutrophils fromperipheralblood blood
9 chr12:123186000-123188600 Flanking Active TSS Monocytes-CD14+_RO01746 blood
10 chr12:123186800-123187800 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
11 chr12:123186800-123188000 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
12 chr12:123187000-123188000 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
13 chr12:123187200-123187800 Flanking Active TSS Adipose Nuclei Adipose
14 chr12:123187400-123187800 Enhancers Primary Natural Killer cells fromperipheralblood blood
15 chr12:123187400-123187800 Enhancers Spleen Spleen
16 chr12:123187400-123188000 Enhancers HMEC breast
17 chr12:123187400-123188200 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
18 chr12:123187400-123188600 Enhancers Hela-S3 cervix
19 chr12:123187600-123187800 Active TSS Foreskin Keratinocyte Primary Cells skin02 Skin
20 chr12:123187600-123187800 Active TSS Esophagus oesophagus
21 chr12:123187600-123187800 Enhancers Fetal Thymus thymus
22 chr12:123187600-123188200 Bivalent Enhancer Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
23 chr12:123187600-123188200 Enhancers HepG2 liver

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