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- W2801693550 endingPage "1597" @default.
- W2801693550 startingPage "1581" @default.
- W2801693550 abstract "Defects in patterning during human embryonic development frequently result in craniofacial abnormalities. The gene regulatory programs that build the craniofacial complex are likely controlled by information located between genes and within intronic sequences. However, systematic identification of regulatory sequences important for forming the human face has not been performed. Here, we describe comprehensive epigenomic annotations from human embryonic craniofacial tissues and systematic comparisons with multiple tissues and cell types. We identified thousands of tissue-specific craniofacial regulatory sequences and likely causal regions for rare craniofacial abnormalities. We demonstrate significant enrichment of common variants associated with orofacial clefting in enhancers active early in embryonic development, while those associated with normal facial variation are enriched near the end of the embryonic period. These data are provided in easily accessible formats for both craniofacial researchers and clinicians to aid future experimental design and interpretation of noncoding variation in those affected by craniofacial abnormalities." @default.
- W2801693550 created "2018-05-17" @default.
- W2801693550 creator A5008052186 @default.
- W2801693550 creator A5034301013 @default.
- W2801693550 creator A5054736588 @default.
- W2801693550 creator A5058778175 @default.
- W2801693550 creator A5085994243 @default.
- W2801693550 date "2018-05-01" @default.
- W2801693550 modified "2023-10-14" @default.
- W2801693550 title "High-Resolution Epigenomic Atlas of Human Embryonic Craniofacial Development" @default.
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