chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
108709204787092048GA6GENIChomozygous52308246
108709221787092218AG17GENIChomozygous51725404
108709243387092434TC9GENIChomozygous51725406
108709380887093809CCA10GENIChomozygous51922199
108709406687094067CT15GENIChomozygous52308248
108709412487094125TC5GENIChomozygous51922203
108709412887094129GGGA6GENIChomozygous52308250
108709424487094245TC9GENIChomozygous51922205
108709454387094544T-1GENIChomozygous51922209
108709466787094668TG9GENICheterozygous51922211
108709469987094700AG11GENIChomozygous51922213
108709476587094766GA6GENIChomozygous51922215
108709495987094960GT12GENICpossibly homozygous52308252
108709508487095085CT17GENICpossibly homozygous51922217
108709520287095203CA16GENIChomozygous52308254
108709556987095570AG17GENICpossibly homozygous51922223
108709586287095863GA10GENIChomozygous51922225
108709588487095899CCTCCACCGAAGCTG---------------3GENICheterozygous52322613
108709673287096733AG6GENIChomozygous51922231
108709673887096739TTA4GENIChomozygous51922233
108709746787097468TC2GENIChomozygous51922237
108709748287097483GA4GENICheterozygous51922239
108709751387097514CT10GENIChomozygous52308258
108709757487097575T-15GENIChomozygous51922241
108709885087098851AG28GENIChomozygous51922245
108709945687099457TC19GENIChomozygous51922247
108709957187099572TC9GENIChomozygous51922251
108709963187099632TC12GENIChomozygous51725418
108709989987099900TC16GENICheterozygous51922253
108709991387099914AAACAC2GENICheterozygous51529799
108709994787099948TC12GENIChomozygous51922255
108709996587099966AG22GENICpossibly homozygous51922257
108710003687100037CT13GENIChomozygous51922259
108710013487100135TA12GENICpossibly homozygous51922261