Variant report

Variant rs150476277
Chromosome Location chr16:30188326-30188327
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:10 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr16:30182600-30194200 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
2 chr16:30185200-30194000 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
3 chr16:30187600-30189200 Enhancers Primary monocytes fromperipheralblood blood
4 chr16:30188000-30188800 Enhancers Cortex derived primary cultured neurospheres brain
5 chr16:30188000-30189200 Enhancers Primary B cells from cord blood blood
6 chr16:30188200-30188400 Flanking Active TSS Primary neutrophils fromperipheralblood blood
7 chr16:30188200-30188400 Enhancers Ganglion Eminence derived primary cultured neurospheres brain
8 chr16:30188200-30188400 Flanking Active TSS Monocytes-CD14+_RO01746 blood
9 chr16:30188200-30189000 Enhancers Primary hematopoietic stem cells short term culture blood
10 chr16:30188200-30189200 Enhancers HepG2 liver

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