Variant report

Variant rs72820499
Chromosome Location chr2:48663080-48663081
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:48660000-48664000 Enhancers Primary monocytes fromperipheralblood blood
2 chr2:48661000-48667200 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
3 chr2:48661400-48666800 Weak transcription Primary hematopoietic stem cells short term culture blood
4 chr2:48661600-48666400 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
5 chr2:48661600-48666400 Weak transcription Fetal Lung lung
6 chr2:48661600-48666600 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
7 chr2:48661600-48667000 Weak transcription Brain Substantia Nigra brain
8 chr2:48661800-48667000 Weak transcription Brain Angular Gyrus brain
9 chr2:48662000-48663800 Enhancers Monocytes-CD14+_RO01746 blood
10 chr2:48662200-48666600 Weak transcription Adipose Nuclei Adipose
11 chr2:48662200-48667000 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
12 chr2:48662200-48667000 Weak transcription Brain Hippocampus Middle brain
13 chr2:48662600-48667000 Weak transcription Liver Liver
14 chr2:48662800-48664000 Enhancers K562 blood
15 chr2:48663000-48663200 Enhancers GM12878-XiMat blood
16 chr2:48663000-48663400 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
17 chr2:48663000-48663400 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
18 chr2:48663000-48664000 Bivalent Enhancer HepG2 liver

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