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. 2022 Aug 22;32(3):402–416. doi: 10.1093/hmg/ddac207

Figure 5.

Figure 5

Progenitor-specific DLK1 putative imprinting at Kagami Ogata syndrome paternal UPD locus. (A) Coverage plot of ATAC-seq in neurons and progenitors at Kagami Ogata syndrome paternal UPD locus. DLK1 showed putative progenitor-specific imprinted expression overlapping the copy number variation. (B) Copy number variation in the 14q32 imprinted gene cluster related to Temple syndrome and Kagami Ogata syndrome. (C) Allelic RNA-seq counts for the SNPs in MEG3 (rs10147988) and MEG8 (rs12879413) in neurons. (D) Allelic RNA-seq counts for the SNPs in MEG3 (rs10147988), MEG8 (rs12879413) and DLK1 in progenitors (rs1802710).