chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
71144781411447816GT22GENICheterozygous141009083
71147820911478210C6GENICheterozygous403200202
71147820911478210CG6GENICheterozygous403200203
71147821811478219C6GENICheterozygous403200204
71147821811478219CG6GENICheterozygous403200205
71148464511484646A10GENICpossibly homozygous403611518
71148464511484646AT10GENICheterozygous403611519
71149398211493983GT11GENICheterozygous154420631
71149398211493983G11GENIChomozygous403200208
71149398311493984TG11GENICheterozygous154420632
71149398311493984T11GENIChomozygous403200209
71149839111498392A8GENICheterozygous403200216
71149839111498392AG8GENIChomozygous403200217
71149839411498395AC8GENIChomozygous141011352
71149839511498396AC7GENIChomozygous141092904
71149895111498952G19GENIChomozygous403200218
71149895111498952GC19GENICheterozygous403200219
71149896511498966A15GENICheterozygous403200220
71149896511498966AC15GENICheterozygous403200221
71149897711498978AG20GENICpossibly homozygous141011353
71149980411499805T19GENICheterozygous403200224
71149980411499805TC19GENIChomozygous403200225
71149981011499811TG18GENIChomozygous138005066