chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3160555348160555349GA34INTERGENIChomozygous57763783
3160555578160555579TC24INTERGENIChomozygous57763784
3160555597160555598CA22INTERGENIChomozygous57763785
3160555919160555920GA13INTERGENIChomozygous57763786
3160556716160556717TC17INTERGENIChomozygous57763789
3160556771160556772CT17INTERGENIChomozygous57763790
3160557141160557142CT21INTERGENIChomozygous57763791
3160557514160557515GC14INTERGENIChomozygous57763793
3160558084160558085TC10INTERGENIChomozygous57763794
3160558094160558095CT13INTERGENIChomozygous57763795
3160558154160558155CT20INTERGENIChomozygous57763796
3160558278160558279TA23INTERGENIChomozygous57763798
3160558348160558349AG30INTERGENICpossibly homozygous57763799
3160558493160558494A-13INTERGENIChomozygous57763800
3160558032160558033TTTACAGATGGTTGTGAGCGTGCTCGCTTCGGCAGCACATATACTAAAATTGGAACGA8INTERGENIChomozygous58630051
3160558176160558180TGTG----16INTERGENIChomozygous58399471
3160558784160558785GT16INTERGENIChomozygous57763801
3160558844160558845TA17INTERGENIChomozygous57763802
3160558931160558932A-10INTERGENIChomozygous57763803
3160559001160559002GA12INTERGENIChomozygous57763804
3160559421160559422GT21INTERGENIChomozygous57763806
3160559681160559682TC20INTERGENIChomozygous57763809
3160560552160560553CG7INTERGENIChomozygous57763810
3160561046160561047TTC20INTERGENIChomozygous57763812
3160561053160561054CCA19INTERGENIChomozygous57763813
3160561479160561480AG22INTERGENIChomozygous57763815
3160561632160561633CT26INTERGENIChomozygous57763816
3160561712160561713CT28INTERGENIChomozygous57763817
3160559534160559535CA26INTERGENIChomozygous58564934