CRISPR CAS Babies: Doubt on the Sanger sequences

Using the new inDelphi (Nature 2018) prediction we can examine the gRNA guided cut used for the CRISPR Baby experiment. The results are somewhat unexpected

Maybe it is difficult to extrapolate from mouse to human embryonic stem cells but one observed event is not even listed here.

The results marked with a star have been observed

The -15 genotype has a probability of less than 0.05%. For +1 genotype the probability is 0.09% and for the -4 deletion it is 3.74%.

Looking therefore again at the Hong Kong slides of He Jiankui, I am getting doubts if the chromatogram  of embryo 2  is correct interpreted even if we admit that the labels of embryo 1 and 2 have been switched..

Color enhanced + sharpened version Hong Kong slide. Unfortunately the chromatograms do not expand to the left also.

Embryo 2 does not show a clean  sequence at all and certainly not a -4/+1 genotype as indicated everywhere “ATTTTCCATACAG-ATTCAATTCTGGACTAAAATAAATACCT” isn’t even a human sequence at all.