chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
6132113820132113821TC9GENIChomozygous54721305
6132113824132113825AG11GENIChomozygous54721307
6132113985132114000TCCTACACACTGTAG---------------2GENIChomozygous54721309
6132114374132114375CT19GENIChomozygous54721311
6132114767132114768GT14GENIChomozygous54721313
6132114807132114808AG5GENIChomozygous54721315
6132114890132114891CT1GENIChomozygous54721317
6132115162132115163CT19GENICpossibly homozygous54721319
6132115700132115701TC13GENIChomozygous54721321
6132115756132115757AG17GENIChomozygous54721323
6132115893132115894AG11GENICheterozygous54721325
6132116023132116024AC4GENIChomozygous54721327
6132116038132116039CA5GENIChomozygous54721329
6132116062132116063TC6GENIChomozygous54721331
6132116068132116069CT5GENIChomozygous54721333
6132116128132116129TTA2GENIChomozygous54721335
6132116561132116562TC8GENIChomozygous54721337
6132117128132117129AG12GENIChomozygous54721341
6132118100132118101AAC6GENIChomozygous54721343
6132123528132123529TC19INTERGENIChomozygous54721355
6132125083132125084GC25INTERGENIChomozygous54721357
6132139191132139192A-1INTERGENIChomozygous54721377
6132140352132140353GA18INTERGENIChomozygous54721379
6132144615132144616AAT4GENIChomozygous54721385
6132145335132145336T-2GENICheterozygous54721387
6132151074132151075TC19GENICpossibly homozygous54721396
6132154635132154636GA14GENICpossibly homozygous54721398
6132163614132163615G-12GENICpossibly homozygous54721406
6132171528132171529TC36GENICpossibly homozygous54721411
6132174353132174354TTG8GENIChomozygous54721413
6132180504132180505C-4GENICheterozygous54721415
6132181020132181021CT19GENIChomozygous54721417
6132182080132182081CT18GENIChomozygous54721420