Variant report

Variant rs16951756
Chromosome Location chr16:79990811-79990812
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:3 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr16:79989600-79992200 Weak transcription Fetal Intestine Small intestine
2 chr16:79989600-79992400 Weak transcription Fetal Intestine Large intestine
3 chr16:79990800-79991000 Bivalent Enhancer hESC Derived CD184+ Endoderm Cultured Cells ES cell derived

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