Variant report

Variant rs112914337
Chromosome Location chr10:829757-829758
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 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 chr10:829400-829800 Bivalent Enhancer Breast Myoepithelial Primary Cells Breast
10 chr10:829400-829800 Flanking Active TSS Pancreas Pancrea
11 chr10:829400-829800 Bivalent Enhancer Skeletal Muscle Female skeletal muscle
12 chr10:829600-829800 Enhancers Brain Angular Gyrus brain
13 chr10:829600-829800 Enhancers Brain Cingulate Gyrus brain
14 chr10:829600-829800 Flanking Active TSS Brain Dorsolateral Prefrontal Cortex brain
15 chr10:829600-829800 Bivalent Enhancer Skeletal Muscle Male skeletal muscle
16 chr10:829600-829800 Enhancers Spleen Spleen
17 chr10:829600-830400 Weak transcription H9 Derived Neuron Cultured Cells ES cell derived
18 chr10:829600-831800 Enhancers Fetal Brain Male brain

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