chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5146438953146438954CCGGGGATTTAGCT17GENIChomozygous56459252
5146438955146438956CA16GENIChomozygous56459253
5146438958146438959TTGGTAGAGCGCTTGC16GENIChomozygous56459254
5146439003146439004AAAAAAG17GENIChomozygous55772885
5146439015146439016GGA23GENICheterozygous56069610
5146441744146441745GA44GENIChomozygous56069611
5146442457146442459AA--16GENICheterozygous55919641
5146442458146442459A-16GENICheterozygous55772889
5146442501146442502A-31GENIChomozygous56069613
5146442883146442884GGA30GENICpossibly homozygous56069614
5146444686146444687TA33GENIChomozygous56069615
5146447477146447478CCCA24GENICpossibly homozygous56069616
5146447812146447813TA12GENIChomozygous56355457
5146447814146447816TT--12GENIChomozygous56355458
5146447816146447817AAGC12GENIChomozygous56459256
5146447824146447825GA12GENIChomozygous55772899
5146447827146447828TA12GENIChomozygous55772901
5146447829146447830CG11GENIChomozygous55772903
5146447831146447832CA11GENIChomozygous55772905
5146447834146447835TG11GENIChomozygous56459257
5146447840146447841TG10GENIChomozygous56459258
5146447841146447842TG9GENIChomozygous56459259
5146447843146447844T-9GENIChomozygous56459260
5146447848146447855CACACTC-------7GENIChomozygous56459261
5146447858146447859AAGGGAGAG7GENIChomozygous56459262
5146447864146447865CG7GENIChomozygous56494600
5146448377146448378GT20GENIChomozygous56069617
5146449261146449262TTACACAC24GENIChomozygous56069620
5146450040146450041CA18GENIChomozygous55772928
5146450041146450042AC18GENIChomozygous56355460
5146451015146451016AAATTCATAT29GENIChomozygous55772934
5146451564146451565CA26GENIChomozygous56069622