chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
35360099153600992CCAT19INTERGENICheterozygous57376279
35360099153600992CCATAT19INTERGENICheterozygous58355512
35360355153603552TC28INTERGENICpossibly homozygous58355514
35360407253604073CCAA15INTERGENIChomozygous58355516
35360775553607757AT--34INTERGENIChomozygous58132551
35361331153613312AT47GENIChomozygous58132567
35361506553615074GCATGGATC---------2GENIChomozygous57376282
35361508853615089TC77GENICheterozygous58132579
35361513553615139TCTT----7GENICheterozygous57376283
35361516853615169TA68GENICheterozygous57376284
35361518653615187TC65GENICheterozygous57376285
35361520953615210GC80GENICheterozygous57376286
35361521453615215C-13GENICheterozygous57376287
35361522953615230GA75GENICheterozygous57376288
35361526153615263GC--3GENICheterozygous57376289
35361959253619593TC141GENICheterozygous58132585
35361961553619616CG89GENICheterozygous57376290
35361961553619616CT93GENICheterozygous57376291
35362227453622275CCAAT26GENIChomozygous58355518
35362295453622955CT37GENIChomozygous58132597
35362499853624999G-30GENIChomozygous57376293
35362500953625010G-30GENIChomozygous57376294
35362505253625053G-30GENIChomozygous57376295
35362505753625058G-31GENIChomozygous57376296
35363099553630996CT37GENIChomozygous58132605
35363480553634806AAT28GENIChomozygous57376297
35363482753634828AAT23GENIChomozygous57376298
35363483253634833GGT23GENIChomozygous57376299
35363496353634964C-49GENIChomozygous57376300
35363623653636237AACC6GENIChomozygous58355520
35363679753636798TC36GENICpossibly homozygous58132620
35363713553637136CA20GENIChomozygous58132622
35363823553638236GA47GENIChomozygous58132624
35363914053639141GA14GENICheterozygous58355522
35364536553645366TA44GENIChomozygous58132628
35364662153646622TC24GENIChomozygous58132634
35364919753649198T-32GENIChomozygous58355524
35365405353654054GGA22GENIChomozygous57376303
35365417353654174GGA46GENIChomozygous57376304