chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
125028588250285883GA22GENIChomozygous115549301
125028775550287756TA29GENIChomozygous115351954
125028836750288368TG15GENIChomozygous115351956
125028908650289087TG17GENIChomozygous115351960
125028947950289480TC30GENIChomozygous115549303
125028979850289799CT37GENIChomozygous115549305
125029234450292345GA23GENIChomozygous115549307
125029256450292565CG42GENIChomozygous115403409
125029785450297855TC37GENICpossibly homozygous115549309
125029934950299350TG16GENIChomozygous115403415
125029942850299429GA22GENIChomozygous115549311
125030009350300094CT31GENICpossibly homozygous115549313
125030058950300590GT30GENICpossibly homozygous115549315
125030060750300608AT28GENICpossibly homozygous115351964
125030180150301802GA16GENIChomozygous115549317
125030550250305503TC21GENIChomozygous115496312
125030569850305699GA22GENICpossibly homozygous115549319
125030622850306229AC20GENIChomozygous115549321
125030657350306574GA20GENIChomozygous115351966
125030772550307726AG22GENICpossibly homozygous115506194
125031137250311373TC28GENIChomozygous115549323
125031137950311380CT30GENIChomozygous115549325
125031143250311433TG37GENIChomozygous115549327
125031157250311573AG40GENIChomozygous115403429
125031328850313289TG42GENICpossibly homozygous115549329