chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3159784186159784187CT29GENIChomozygous111790343
3159785953159785954AG13GENIChomozygous111790345
3159786499159786500TC24GENIChomozygous111790347
3159786564159786565AG26GENIChomozygous111790349
3159787310159787311TC25GENIChomozygous111790357
3159787316159787317CT25GENIChomozygous111790359
3159787460159787461TA28GENIChomozygous111790361
3159788175159788176AG30GENIChomozygous111790363
3159788250159788251AC23GENIChomozygous111790365
3159788337159788338GA26GENIChomozygous111790367
3159788870159788871TC20GENIChomozygous111790369
3159788942159788943AG19GENIChomozygous111790371
3159793821159793822CT33GENIChomozygous111790387
3159793982159793983AG23GENIChomozygous111790389
3159794347159794348CT27GENIChomozygous111790391
3159794505159794506CT35GENIChomozygous111790393
3159794572159794573CG34GENIChomozygous111790395
3159794623159794624CT36GENIChomozygous111790397
3159795664159795665TC18GENIChomozygous111790399
3159797908159797909GA16GENIChomozygous111790401
3159798461159798462CT23GENIChomozygous111790403
3159798600159798601CT26GENIChomozygous111790405
3159799387159799388TC24GENIChomozygous111790407
3159799423159799424CA35GENIChomozygous111790409
3159799578159799579GA36GENIChomozygous111790411
3159799981159799982TG31GENIChomozygous111790415
3159800335159800336GA22GENIChomozygous111790417
3159800844159800845TC20GENIChomozygous111790419
3159800944159800945AG24GENIChomozygous111790421
3159801828159801829AG32GENIChomozygous111790423