Variant report

Variant rs6956488
Chromosome Location chr7:153638488-153638489
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:10 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr7:153628200-153640600 Weak transcription Stomach Smooth Muscle stomach
2 chr7:153631000-153643000 Weak transcription Right Atrium heart
3 chr7:153632200-153641200 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
4 chr7:153637000-153640200 Weak transcription Fetal Kidney kidney
5 chr7:153638000-153638600 Enhancers Pancreatic Islets Pancreatic Islet
6 chr7:153638200-153638600 Enhancers Gastric stomach
7 chr7:153638200-153640200 Enhancers Ganglion Eminence derived primary cultured neurospheres brain
8 chr7:153638400-153638600 Bivalent Enhancer Fetal Brain Female brain
9 chr7:153638400-153639000 Bivalent Enhancer Fetal Brain Male brain
10 chr7:153638400-153640400 Enhancers Brain Germinal Matrix brain

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