chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3159784186159784187CT32GENIChomozygous111790343
3159785953159785954AG17GENIChomozygous111790345
3159786499159786500TC24GENIChomozygous111790347
3159786564159786565AG19GENIChomozygous111790349
3159786639159786640GA25GENIChomozygous111790351
3159786915159786916CT9GENIChomozygous111790353
3159787310159787311TC17GENIChomozygous111790357
3159787316159787317CT17GENIChomozygous111790359
3159787460159787461TA21GENIChomozygous111790361
3159788175159788176AG26GENIChomozygous111790363
3159788250159788251AC18GENIChomozygous111790365
3159788337159788338GA26GENIChomozygous111790367
3159788870159788871TC24GENIChomozygous111790369
3159793821159793822CT23GENIChomozygous111790387
3159793982159793983AG22GENIChomozygous111790389
3159794347159794348CT23GENIChomozygous111790391
3159794572159794573CG25GENIChomozygous111790395
3159794623159794624CT25GENIChomozygous111790397
3159795664159795665TC16GENIChomozygous111790399
3159797908159797909GA20GENIChomozygous111790401
3159798461159798462CT22GENIChomozygous111790403
3159798600159798601CT23GENIChomozygous111790405
3159799387159799388TC30GENIChomozygous111790407
3159799423159799424CA26GENIChomozygous111790409
3159799578159799579GA23GENIChomozygous111790411
3159799981159799982TG36GENIChomozygous111790415
3159800335159800336GA26GENIChomozygous111790417
3159800844159800845TC19GENIChomozygous111790419
3159800944159800945AG34GENIChomozygous111790421
3159801828159801829AG26GENIChomozygous111790423