chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5158442110158442111TC-1GENIC182576483
5158442742158442743TC-1GENIC182576484
5158442959158442960CT-1GENIC181714487
5158443409158443410TC-1GENIC181714488
5158444831158444832TC-1GENIC182576485
5158444846158444847TC-1GENIC182576486
5158445001158445002GC-1GENIC182576487
5158445621158445622TC-1GENIC181714489
5158445974158445975GA-1GENIC182576488
5158446898158446899GT-1GENIC182576489
5158447033158447034TC-1GENIC182576490
5158447141158447142CT-1GENIC182576491
5158447413158447414AG-1GENIC182576492
5158448718158448719GC-1GENIC182576493
5158448875158448876CT-1GENIC182576494
5158448903158448904AG-1GENIC182576495
5158448987158448988CT-1GENIC182576496
5158449427158449428TA-1GENIC182576497
5158449606158449607GA-1GENIC182576498
5158449709158449710TG-1GENIC181714490
5158450063158450064AG-1GENIC182576499
5158450514158450515AT-1GENIC181714491
5158450993158450994TC-1GENIC182576500
5158451054158451055TC-1GENIC182576501
5158451214158451215AG-1GENIC182576502
5158452691158452692CT-1GENIC181714492
5158453039158453040GT-1GENIC182576503