Variant report

Variant rs55669814
Chromosome Location chr13:97782316-97782317
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr13:97774000-97784400 Enhancers Placenta Placenta
2 chr13:97777200-97783400 Weak transcription K562 blood
3 chr13:97778600-97784000 Weak transcription hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
4 chr13:97778800-97783600 Weak transcription H9 Derived Neuron Cultured Cells ES cell derived
5 chr13:97778800-97783800 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
6 chr13:97778800-97783800 Weak transcription Brain Substantia Nigra brain
7 chr13:97778800-97788200 Weak transcription Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
8 chr13:97779000-97786200 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
9 chr13:97779000-97788400 Weak transcription Brain Cingulate Gyrus brain
10 chr13:97779200-97782400 Weak transcription NHDF-Ad bronchial
11 chr13:97779200-97785600 Weak transcription Lung lung
12 chr13:97781200-97785400 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
13 chr13:97781800-97782800 Enhancers Breast Myoepithelial Primary Cells Breast
14 chr13:97782200-97783400 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived

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