chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4241020341241020342AT34GENICheterozygous57161721
4241020395241020396TC33GENICheterozygous57161724
4241020471241020472GC31GENICheterozygous57161727
4241020506241020507GA29GENICheterozygous57161729
4241020780241020781GA16GENICheterozygous57161732
4241020791241020792GA13GENICheterozygous57161735
4241020839241020840AT9GENICheterozygous57161738
4241021389241021390AG22GENICheterozygous57161744
4241021396241021397AC21GENICheterozygous57161748
4241021625241021626TA34GENICheterozygous57161751
4241024389241024390GA38GENICheterozygous57161790
4241028953241028954TC20GENICheterozygous57161851
4241030577241030578TC24GENICheterozygous57161860
4241042504241042505TTA30GENICheterozygous57162096
4241044343241044344AG7GENICheterozygous57162111
4241045151241045152GA11GENICheterozygous57162126
4241045193241045194GT15GENICheterozygous57162129
4241070840241070841CG6GENICheterozygous57162354
4241116941241116942C-15GENICheterozygous57162989
4241117009241117010CG20GENICheterozygous57162991
4241117044241117045TA20GENICheterozygous57162994
4241117076241117077G-21GENICheterozygous57162997