Variant report

Variant rs76796544
Chromosome Location chr6:162529941-162529942
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:10 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:162525200-162539800 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
2 chr6:162529000-162530000 Enhancers H9 Derived Neuron Cultured Cells ES cell derived
3 chr6:162529200-162530000 Enhancers Pancreas Pancrea
4 chr6:162529200-162530200 Enhancers H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
5 chr6:162529200-162530600 Enhancers Brain Inferior Temporal Lobe brain
6 chr6:162529400-162530000 Enhancers ES-I3 Cell Line embryonic stem cell
7 chr6:162529800-162530600 Enhancers Left Ventricle heart
8 chr6:162529800-162530600 Enhancers Skeletal Muscle Male skeletal muscle
9 chr6:162529800-162530800 Enhancers Foreskin Fibroblast Primary Cells skin02 Skin
10 chr6:162529800-162531000 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin

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