chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X2551478825514789AC14GENIChomozygous62926709
X2551615525516156CT11GENIChomozygous62926710
X2551632525516326TG13GENIChomozygous62926711
X2551653825516539TC11GENIChomozygous62926712
X2552234725522348TG7GENIChomozygous62926713
X2552406725524068TC12GENIChomozygous62926714
X2552601525526016GA13GENIChomozygous62926715
X2552717825527179GA10GENIChomozygous62926716
X2552767425527675TC9GENIChomozygous62926717
X2553029525530296AG17GENIChomozygous62926718
X2553306725533068GA8GENIChomozygous62926719
X2553371525533716GA12GENIChomozygous62926720
X2553398925533990AG8GENIChomozygous62926721
X2553484825534849AG8GENIChomozygous62926722
X2553589625535897GA8GENIChomozygous62926723
X2553776225537763AG12GENIChomozygous62926726
X2553911125539112TC20GENIChomozygous62926727
X2553917925539180TC12GENIChomozygous62926728
X2553933825539339CT11GENIChomozygous62926729
X2553998325539984AG6GENIChomozygous62926730
X2554004425540045CT4GENICheterozygous62926731
X2554251025542511TC9GENIChomozygous62926732
X2554284125542842GT6GENIChomozygous62926733
X2554355825543559TC9GENIChomozygous62926734
X2554447825544479AT11GENIChomozygous62926735
X2554543025545431GA9GENIChomozygous62926736
X2554615025546151CT12GENIChomozygous62926737
X2554637125546372TC7GENIChomozygous62926738
X2554674825546749CT8GENIChomozygous62926739