Variant report

Variant rs7782005
Chromosome Location chr7:111029564-111029565
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr7:111012600-111033000 Weak transcription Aorta Aorta
2 chr7:111016600-111032600 Weak transcription Psoas Muscle Psoas
3 chr7:111021400-111032800 Weak transcription Pancreas Pancrea
4 chr7:111022000-111032000 Weak transcription Fetal Kidney kidney
5 chr7:111023800-111032800 Weak transcription Duodenum Smooth Muscle Duodenum
6 chr7:111024000-111036400 Weak transcription Right Ventricle heart
7 chr7:111024400-111031200 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
8 chr7:111025200-111032600 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
9 chr7:111025200-111033000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
10 chr7:111026200-111031400 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
11 chr7:111026800-111031200 Weak transcription Breast Myoepithelial Primary Cells Breast
12 chr7:111027000-111030000 Weak transcription Pancreatic Islets Pancreatic Islet
13 chr7:111028000-111032600 Weak transcription Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
14 chr7:111028400-111032600 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
15 chr7:111028600-111029600 Enhancers Primary B cells from peripheral blood blood
16 chr7:111029200-111032800 Weak transcription Ovary ovary
17 chr7:111029400-111029800 Enhancers GM12878-XiMat blood

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