chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
108709204787092048GA7GENIChomozygous52308246
108709221787092218AG15GENIChomozygous51725404
108709243387092434TC19GENIChomozygous51725406
108709380887093809CCA19GENIChomozygous51922199
108709406687094067CT21GENIChomozygous52308248
108709412487094125TC4GENIChomozygous51922203
108709412887094129GGGA6GENIChomozygous52308250
108709424487094245TC15GENICpossibly homozygous51922205
108709454387094544T-4GENICheterozygous51922209
108709466787094668TG15GENICpossibly homozygous51922211
108709469987094700AG9GENICpossibly homozygous51922213
108709476587094766GA6GENIChomozygous51922215
108709495987094960GT19GENIChomozygous52308252
108709508487095085CT24GENIChomozygous51922217
108709520287095203CA20GENIChomozygous52308254
108709556987095570AG28GENICpossibly homozygous51922223
108709586287095863GA12GENIChomozygous51922225
108709588487095899CCTCCACCGAAGCTG---------------4GENICheterozygous52322613
108709673287096733AG7GENICheterozygous51922231
108709673887096739TTA7GENICheterozygous51922233
108709745387097454GA1GENIChomozygous52308256
108709746787097468TC1GENIChomozygous51922237
108709748287097483GA5GENIChomozygous51922239
108709751387097514CT16GENICpossibly homozygous52308258
108709757487097575T-13GENICpossibly homozygous51922241
108709885087098851AG24GENIChomozygous51922245
108709945687099457TC25GENIChomozygous51922247
108709957187099572TC17GENIChomozygous51922251
108709963187099632TC20GENICheterozygous51725418
108709989987099900TC20GENICheterozygous51922253
108709991387099914AAACAC1GENIChomozygous51529799
108709994787099948TC9GENIChomozygous51922255
108709996587099966AG22GENICpossibly homozygous51922257
108710003687100037CT19GENIChomozygous51922259
108710013487100135TA22GENIChomozygous51922261