Variant report

Variant rs9875513
Chromosome Location chr3:51570924-51570925
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr3:51563200-51572000 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
2 chr3:51568800-51572000 Enhancers Placenta Placenta
3 chr3:51570000-51571800 Weak transcription Liver Liver
4 chr3:51570000-51572000 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
5 chr3:51570400-51571400 Weak transcription Placenta Amnion Placenta Amnion
6 chr3:51570600-51571000 Weak transcription Lung lung
7 chr3:51570600-51571200 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
8 chr3:51570600-51571600 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
9 chr3:51570600-51571600 Weak transcription HMEC breast
10 chr3:51570600-51571600 Weak transcription NHEK skin
11 chr3:51570600-51571600 Weak transcription Osteobl bone
12 chr3:51570600-51571800 Enhancers Foreskin Fibroblast Primary Cells skin02 Skin
13 chr3:51570600-51572000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
14 chr3:51570800-51571000 Enhancers Primary hematopoietic stem cells short term culture blood
15 chr3:51570800-51571600 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
16 chr3:51570800-51572000 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
17 chr3:51570800-51572000 Enhancers GM12878-XiMat blood

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