chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5143649841143649842GA16GENIChomozygous663546272
5143650275143650276CT22GENIChomozygous663546273
5143650874143650875T-12GENIChomozygous765204629
5143652921143652922CCT19GENIChomozygous765204630
5143653053143653054TA13GENIChomozygous663546274
5143653704143653706TT--5GENICheterozygous765204631
5143653705143653706T-5GENICheterozygous765204632
5143653825143653828TTT---14GENIChomozygous765204633
5143653991143653992AG11GENIChomozygous663546275
5143654022143654023CT9GENIChomozygous663546276
5143654077143654078TA9GENIChomozygous663546277
5143654078143654079TA9GENIChomozygous663546278
5143654080143654081TA11GENIChomozygous663546279
5143654087143654088TTA11GENICheterozygous765204635
5143654168143654169AG22GENIChomozygous663546280
5143654180143654181CG20GENIChomozygous663546281
5143654658143654659AG19GENIChomozygous663546282
5143656319143656320TC31GENIChomozygous663546283
5143657627143657628AAC8GENIChomozygous765204636
5143657632143657634GC--9GENIChomozygous765204637
5143657643143657644TTC7GENIChomozygous765204638
5143657653143657654A-7GENIChomozygous765204639
5143657656143657658CT--7GENIChomozygous765204640
5143657836143657837G-24GENIChomozygous765204641
5143659534143659536TA--6GENIChomozygous765204642
5143659541143659551TTATTATTAT----------8GENIChomozygous765204643
5143663154143663155TTTGTG5GENIChomozygous765204647
5143663745143663746CCAA3GENIChomozygous765204648
5143663904143663905AG23GENIChomozygous663546284
5143664036143664037A-21GENIChomozygous765204650
5143664037143664038AT21GENIChomozygous663546285
5143664536143664537AG29GENIChomozygous663546286