Variant report

Variant rs12366014
Chromosome Location chr11:45559793-45559794
allele A/T
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr11:45540200-45560200 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
2 chr11:45554200-45570600 Weak transcription Brain Germinal Matrix brain
3 chr11:45554600-45563000 Weak transcription Brain Angular Gyrus brain
4 chr11:45554800-45563000 Weak transcription Brain Inferior Temporal Lobe brain
5 chr11:45556200-45571200 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
6 chr11:45558600-45559800 Weak transcription Fetal Brain Female brain
7 chr11:45558800-45562600 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
8 chr11:45559000-45560800 Enhancers Osteobl bone
9 chr11:45559000-45561200 Enhancers H1 Derived Mesenchymal Stem Cells ES cell derived
10 chr11:45559200-45560400 Bivalent Enhancer Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
11 chr11:45559200-45560600 Bivalent Enhancer Fetal Stomach stomach
12 chr11:45559200-45561400 Enhancers Fetal Brain Male brain
13 chr11:45559400-45560000 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
14 chr11:45559600-45559800 Bivalent Enhancer Foreskin Fibroblast Primary Cells skin01 Skin
15 chr11:45559600-45559800 Active TSS Brain Dorsolateral Prefrontal Cortex brain
16 chr11:45559600-45560400 Enhancers Brain Anterior Caudate brain
17 chr11:45559600-45560400 Enhancers Fetal Muscle Trunk muscle

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