Variant report

Variant rs554333526
Chromosome Location chr10:829453-829454
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr10:818400-830600 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
2 chr10:822000-830400 Weak transcription Esophagus oesophagus
3 chr10:825400-830400 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
4 chr10:825400-830400 Weak transcription NH-A brain
5 chr10:828800-829800 Enhancers iPS DF 19.11 Cell Line embryonic stem cell
6 chr10:828800-831200 Weak transcription Fetal Heart heart
7 chr10:829000-829800 Enhancers Brain Inferior Temporal Lobe brain
8 chr10:829200-830400 Enhancers Ovary ovary
9 chr10:829400-829600 Enhancers H9 Derived Neuron Cultured Cells ES cell derived
10 chr10:829400-829600 Bivalent/Poised TSS Foreskin Melanocyte Primary Cells skin01 Skin
11 chr10:829400-829600 Enhancers Brain Dorsolateral Prefrontal Cortex brain
12 chr10:829400-829600 Enhancers Lung lung
13 chr10:829400-829600 Bivalent Enhancer HepG2 liver
14 chr10:829400-829800 Bivalent Enhancer Breast Myoepithelial Primary Cells Breast
15 chr10:829400-829800 Flanking Active TSS Pancreas Pancrea
16 chr10:829400-829800 Bivalent Enhancer Skeletal Muscle Female skeletal muscle

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