chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2114442505114442506A-5GENIChomozygous59030010
2114444448114444449TTAAAA5GENIChomozygous59846946
2114444816114444817GA21GENICpossibly homozygous59846947
2114445515114445519GTTT----18GENIChomozygous59030015
2114446038114446039AG20GENIChomozygous59030016
2114446278114446279CA14GENIChomozygous59030018
2114447053114447054TC31GENIChomozygous59030019
2114447098114447099AG30GENIChomozygous59030020
2114447254114447258TTTT----9GENICheterozygous59030021
2114447275114447279GGTC----13GENICheterozygous59030022
2114447275114447277GG--13GENICheterozygous59030023
2114447753114447754GA23GENIChomozygous59030024
2114448477114448478CT21GENIChomozygous59030025
2114448722114448723AAG28GENIChomozygous59846948
2114448845114448846TTTGTGGGAAGAA12GENIChomozygous59030026
2114449119114449120CCA4GENIChomozygous59030027
2114449130114449131GA3GENIChomozygous59030028
2114449189114449190GGA7GENIChomozygous59030029
2114450362114450363TC22GENIChomozygous59030030
2114451127114451128CA30GENICpossibly homozygous59030033
2114451631114451632TC22GENIChomozygous59030034
2114451797114451798TTACG23GENIChomozygous59030035
2114452519114452520G-16GENIChomozygous59030036
2114454341114454342GGT24GENIChomozygous59030037
2114470079114470081GA--6GENIChomozygous59030038
2114470082114470083G-16GENIChomozygous59030039
2114471927114471928AG9GENIChomozygous59030040
2114471994114471995A-16GENIChomozygous59846950
2114472776114472777CT30GENIChomozygous59846951
2114473024114473025GA39GENIChomozygous59030041
2114473086114473087AC42GENIChomozygous59030042
2114473800114473801GA19GENIChomozygous59030043
2114473984114473985CT16GENIChomozygous59030044
2114475969114475970AAT21GENIChomozygous59030046
2114476064114476069TTATT-----10GENIChomozygous59030047
2114476210114476212AA--30GENIChomozygous59030048
2114476263114476265TG--25GENIChomozygous59030049
2114476614114476615GA11GENIChomozygous59030052
2114478297114478298GA16GENIChomozygous59030054
2114479657114479658AG15GENIChomozygous59030055