chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
36692623366926234AG20GENIChomozygous58549132
36692693366926934AATGGATGGATGGG13GENIChomozygous58549133
36692696266926963TC12GENIChomozygous57419888
36692802366928024TTTC20GENICpossibly homozygous58549134
36692819766928198CT24GENIChomozygous58549135
36692830666928307CT22GENIChomozygous58549136
36692832966928330GA17GENIChomozygous58549137
36692939066929391CA13GENIChomozygous58549138
36692940166929403TT--15GENIChomozygous58549139
36692940366929404TG14GENIChomozygous58549140
36692944566929446AG14GENIChomozygous57419896
36692964566929646CA16GENIChomozygous58549141
36692990466929905CT20GENIChomozygous57419898
36693031166930312GA9GENIChomozygous57419899
36693071266930713GA17GENIChomozygous57419907
36693227566932276TG6GENIChomozygous58549142
36693315166933152AACGCACCAT6GENIChomozygous58549143
36693408666934087CCAT33GENIChomozygous57419921
36693443166934432GA24GENIChomozygous57419927
36693606466936065TC21GENIChomozygous57419939
36693693166936932GC22GENIChomozygous57419951
36693447466934475CCAT16GENICpossibly homozygous58590994
36693933466939335TC14GENIChomozygous57419971
36693963666939637AATG18GENIChomozygous57419973
36694015566940156TTA7GENICpossibly homozygous58549145
36694059866940599TC6GENIChomozygous57419983