Variant report

Variant rs11784242
Chromosome Location chr8:120449997-120449998
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:12 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr8:120441000-120450000 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
2 chr8:120443200-120450000 Weak transcription Aorta Aorta
3 chr8:120448200-120450400 Enhancers NHDF-Ad bronchial
4 chr8:120448400-120451200 Enhancers Fetal Muscle Leg muscle
5 chr8:120448400-120452800 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
6 chr8:120448600-120451400 Enhancers Fetal Stomach stomach
7 chr8:120449400-120450400 Enhancers H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
8 chr8:120449400-120450400 Enhancers H9 Derived Neuron Cultured Cells ES cell derived
9 chr8:120449600-120450200 Enhancers Liver Liver
10 chr8:120449800-120450000 Enhancers Cortex derived primary cultured neurospheres brain
11 chr8:120449800-120450200 Active TSS Fetal Lung lung
12 chr8:120449800-120451200 Weak transcription Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow

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