Variant report

Variant rs2936739
Chromosome Location chr12:123185929-123185930
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:21 , 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 chr12:123185200-123186000 Active TSS Primary neutrophils fromperipheralblood blood
5 chr12:123185200-123186000 Enhancers HMEC breast
6 chr12:123185200-123186000 Enhancers Monocytes-CD14+_RO01746 blood
7 chr12:123185200-123187200 Active TSS Esophagus oesophagus
8 chr12:123185400-123186200 Active TSS Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
9 chr12:123185400-123186800 Active TSS Primary hematopoietic stem cells blood
10 chr12:123185400-123188200 Active TSS Primary B cells from cord blood blood
11 chr12:123185600-123186000 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
12 chr12:123185600-123186000 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
13 chr12:123185600-123186000 Weak transcription Placenta Placenta
14 chr12:123185800-123186000 Enhancers ES-I3 Cell Line embryonic stem cell
15 chr12:123185800-123186000 Flanking Active TSS Foreskin Keratinocyte Primary Cells skin02 Skin
16 chr12:123185800-123186000 Flanking Active TSS NHEK skin
17 chr12:123185800-123186200 Enhancers hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
18 chr12:123185800-123186200 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
19 chr12:123185800-123186400 Bivalent Enhancer IMR90 fetal lung fibroblasts Cell Line lung
20 chr12:123185800-123186400 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
21 chr12:123185800-123187000 Flanking Active TSS Adipose Nuclei Adipose

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