chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
57504976975049770GA19INTERGENIChomozygous55470299
57505041875050419GA14INTERGENIChomozygous55470300
57505049475050495GA11INTERGENIChomozygous55470301
57505068575050686AT23INTERGENIChomozygous55470302
57505080075050801AG14INTERGENIChomozygous55470303
57505080975050810CT15INTERGENIChomozygous55470304
57505088575050886CG19INTERGENIChomozygous55470305
57505158375051584TG15INTERGENIChomozygous55470306
57505175475051755AG18INTERGENIChomozygous55470307
57505186975051870TC23INTERGENIChomozygous55470308
57505225275052253TC22INTERGENIChomozygous55470309
57505228475052285TC26INTERGENIChomozygous55470310
57505242375052424CT23INTERGENIChomozygous55470311
57505247575052476TA28INTERGENIChomozygous55470312
57505332875053329GA20INTERGENIChomozygous55470314
57505337475053375AG13INTERGENIChomozygous55470315
57505353575053536TTAC16INTERGENIChomozygous55470316
57505367075053671CG15INTERGENIChomozygous55470317
57505397575053976T-16INTERGENIChomozygous55470318
57505455075054551TC12INTERGENIChomozygous55470319
57505455175054552GA12INTERGENIChomozygous55470320
57505455475054555CCT11INTERGENIChomozygous55885118