SNCA and Parkinson disease: Here, we demonstrate that numerous genes implicated in autosomal human genetic diseases, such as Parkinson (DNAJC6, LRRK2 and SNCA), epilepsy (SCN1A, GABR1, and SAMD12), deafness (ATP11A, EPS8, and MYO6), and neurodevelopmental disorders (KCNA1, RETREG1, ROBO1, and TIAM1), are located within VERT regions and display AEI.