Variant report

Variant rs61798079
Chromosome Location chr3:178496515-178496516
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr3:178482000-178507000 Weak transcription Pancreatic Islets Pancreatic Islet
2 chr3:178495000-178496600 Enhancers Muscle Satellite Cultured Cells --
3 chr3:178495200-178496600 Enhancers GM12878-XiMat blood
4 chr3:178495200-178496800 Enhancers HMEC breast
5 chr3:178495200-178496800 Enhancers HSMMtube muscle
6 chr3:178495200-178496800 Enhancers NHEK skin
7 chr3:178495200-178497000 Enhancers HSMM muscle
8 chr3:178495400-178496800 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
9 chr3:178495400-178496800 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
10 chr3:178495800-178496600 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
11 chr3:178496200-178496600 Enhancers Left Ventricle heart
12 chr3:178496200-178497000 Enhancers Gastric stomach
13 chr3:178496400-178502000 Weak transcription Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
14 chr3:178496400-178502600 Weak transcription H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived

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