Variant report

Variant rs10769159
Chromosome Location chr11:45688595-45688596
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr11:45687200-45689400 Enhancers HSMMtube muscle
2 chr11:45687200-45699000 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
3 chr11:45687600-45688800 Enhancers Brain Inferior Temporal Lobe brain
4 chr11:45687600-45688800 Enhancers Brain Substantia Nigra brain
5 chr11:45687600-45689000 Bivalent Enhancer Fetal Muscle Trunk muscle
6 chr11:45687600-45689000 Bivalent Enhancer Fetal Muscle Leg muscle
7 chr11:45687600-45689600 Bivalent Enhancer Fetal Stomach stomach
8 chr11:45687600-45692000 Weak transcription Pancreas Pancrea
9 chr11:45687800-45688800 Enhancers Brain Angular Gyrus brain
10 chr11:45687800-45688800 Enhancers Brain Anterior Caudate brain
11 chr11:45687800-45688800 Enhancers Brain Dorsolateral Prefrontal Cortex brain
12 chr11:45687800-45689000 Enhancers Brain Hippocampus Middle brain
13 chr11:45687800-45692400 Weak transcription Breast Myoepithelial Primary Cells Breast
14 chr11:45688000-45700600 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
15 chr11:45688200-45688800 Enhancers Fetal Brain Female brain
16 chr11:45688200-45689000 Enhancers Brain Cingulate Gyrus brain
17 chr11:45688400-45688800 Enhancers iPS DF 19.11 Cell Line embryonic stem cell

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