chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
29112672991126730AG13GENIChomozygous109909952
29112963791129638AC44GENIChomozygous109909954
29113018791130188GT26GENIChomozygous109909956
29113030591130306AT15GENIChomozygous109909958
29113040391130404AT16GENIChomozygous120125575
29113274091132741TC20GENIChomozygous109909970
29113334591133346AG19GENIChomozygous109909972
29113418491134185CT27GENIChomozygous109909974
29113431091134311AG23GENIChomozygous109909976
29113455491134555TC17GENIChomozygous109909978
29113492591134926TA24GENIChomozygous109909980
29113575591135756GA32GENIChomozygous109909982
29113576691135767TC34GENIChomozygous109909984
29113676791136768GC31GENIChomozygous109909986
29113677991136780CT33GENIChomozygous109909988
29113762591137626CT9GENIChomozygous109909990
29113813691138137AC7GENIChomozygous109909992
29113815391138154TG8GENIChomozygous109909994
29113858891138589GA8GENIChomozygous109909996
29113961091139611TG13GENIChomozygous109909998
29114021691140217GA11GENIChomozygous109910000
29114029991140300TC6GENIChomozygous109910002
29114058591140586GA20GENIChomozygous109910004
29114233591142336CT26GENIChomozygous109910006
29114243791142438CG25GENIChomozygous109910008
29114327191143272GT17GENIChomozygous109910010
29114331691143317CT20GENIChomozygous109910012
29114345091143451TC22GENIChomozygous109910014
29114404591144046TA25GENIChomozygous109910016
29114414791144148GT20GENIChomozygous109910018
29114422591144226GT24GENIChomozygous109910020
29114480991144810TA12GENIChomozygous109910024
29114575291145753CA49GENIChomozygous109910026
29114867091148671CA39GENIChomozygous109910052