Variant report

Variant rs11038466
Chromosome Location chr11:45457902-45457903
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr11:45447800-45462400 Weak transcription Fetal Brain Male brain
2 chr11:45457000-45466200 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
3 chr11:45457200-45458000 Bivalent Enhancer Fetal Stomach stomach
4 chr11:45457200-45458200 Enhancers Brain Germinal Matrix brain
5 chr11:45457200-45459200 Enhancers Skeletal Muscle Male skeletal muscle
6 chr11:45457400-45458000 Bivalent Enhancer Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
7 chr11:45457400-45458000 Bivalent Enhancer Brain Substantia Nigra brain
8 chr11:45457400-45458400 Bivalent Enhancer Brain Hippocampus Middle brain
9 chr11:45457400-45458600 Enhancers Brain Anterior Caudate brain
10 chr11:45457400-45459000 Enhancers Brain Cingulate Gyrus brain
11 chr11:45457400-45459200 Enhancers Brain Angular Gyrus brain
12 chr11:45457400-45459200 Enhancers Brain Dorsolateral Prefrontal Cortex brain
13 chr11:45457600-45459000 Weak transcription Brain Inferior Temporal Lobe brain
14 chr11:45457800-45458200 Bivalent Enhancer Osteobl bone

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