chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
116871036568710367CA--7INTERGENICheterozygous51217917
116872979968729800C-10INTERGENICheterozygous51217919
116874566968745670GGC9INTERGENIChomozygous50813075
116875070068750701CT15INTERGENIChomozygous50813107
116875252668752528GT--8INTERGENICheterozygous51187689
116876223168762235TTGA----9INTERGENICheterozygous51196727
116877305168773052A-8INTERGENICheterozygous51288021
116878873268788733C-15INTERGENIChomozygous50813354
116879272268792723GGA15INTERGENICpossibly homozygous51294882
116880444868804449T-9INTERGENICheterozygous51202353
116880716268807163C-6INTERGENICheterozygous50813453
116881216968812170CCT21INTERGENIChomozygous50813463
116881217468812175AAT22INTERGENIChomozygous51166532
116881218368812184CA24INTERGENIChomozygous51187695
116881220968812210GGT21INTERGENIChomozygous50813465
116881223768812238AAT21INTERGENIChomozygous51187696
116881226068812261CCT17INTERGENIChomozygous50813467
116881226668812267G-17INTERGENIChomozygous50813469
116881227468812275AAT15INTERGENIChomozygous50813471
116881227868812279T-17INTERGENIChomozygous50813473
116881528568815287GT--7INTERGENICheterozygous51187697
116881647268816474GT--22INTERGENICheterozygous51196730
116881704568817049TGTG----13INTERGENICheterozygous51217929
116881704768817049TG--13INTERGENICpossibly homozygous51187698
116881884168818842C-32INTERGENIChomozygous50813491
116882671368826714AAGAGAG19INTERGENICheterozygous51284071
116884119568841196AATTTC26INTERGENIChomozygous50813601
116884133568841336CCA24GENIChomozygous50813603