chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2247515710247515711GA28GENIChomozygous110365280
2247515728247515729AG29GENIChomozygous110365282
2247515800247515801CT30GENIChomozygous110365284
2247515830247515831CT29GENIChomozygous110365286
2247516059247516060GA19GENIChomozygous110365288
2247516254247516255CA11GENIChomozygous110365290
2247516389247516390AG29GENIChomozygous110365292
2247516425247516426CT34GENIChomozygous110365294
2247523775247523776AC12GENIChomozygous110365296
2247523880247523881TA8GENIChomozygous110634489
2247523916247523917GA11GENIChomozygous110365298
2247523925247523926TA13GENIChomozygous110365300
2247524179247524180AG24GENIChomozygous110365304
2247524234247524235CT18GENIChomozygous110365306
2247524293247524294CA17GENIChomozygous110365308
2247524382247524383GA12GENIChomozygous110365310
2247524506247524507TC17GENIChomozygous110365312
2247524678247524679AC35GENIChomozygous110365314
2247524739247524740GA23GENIChomozygous110365316
2247524816247524817CG24GENIChomozygous110365318
2247524876247524877TC12GENIChomozygous110365320
2247524915247524916CT14GENIChomozygous110365322
2247525327247525328CT35GENIChomozygous110365324
2247525507247525508GC21GENIChomozygous110365326
2247525537247525538GA25GENIChomozygous110365328
2247525558247525559TC29GENIChomozygous110365330
2247525619247525620TC26GENIChomozygous110365332
2247525748247525749CT6GENIChomozygous110365334
2247525767247525768CT4GENIChomozygous110365336
2247525893247525894CT5GENIChomozygous110365338
2247525945247525946TC4GENIChomozygous110365340