Variant report

Variant rs59311846
Chromosome Location chr16:48137555-48137556
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr16:48131800-48138600 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
2 chr16:48135000-48137800 Enhancers Skeletal Muscle Male skeletal muscle
3 chr16:48135200-48139000 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
4 chr16:48135600-48137800 Enhancers GM12878-XiMat blood
5 chr16:48135800-48140000 Weak transcription Fetal Brain Male brain
6 chr16:48136200-48141600 Enhancers hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
7 chr16:48136400-48137800 Enhancers Left Ventricle heart
8 chr16:48136400-48139800 Weak transcription Cortex derived primary cultured neurospheres brain
9 chr16:48136600-48138000 Enhancers Skeletal Muscle Female skeletal muscle
10 chr16:48136800-48137600 Weak transcription Pancreas Pancrea
11 chr16:48137000-48137800 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
12 chr16:48137000-48138000 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
13 chr16:48137400-48137600 Enhancers Right Ventricle heart
14 chr16:48137400-48137800 Enhancers H1 Cell Line embryonic stem cell

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