chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1261338174261338175AC19GENIChomozygous108629357
1261339472261339473AT30GENIChomozygous108629358
1261341260261341261AG33GENIChomozygous108629361
1261341373261341374CT28GENIChomozygous109025994
1261342554261342555AG25GENIChomozygous108629363
1261343000261343001CT20GENIChomozygous109025995
1261344363261344364AC35GENIChomozygous108629365
1261348114261348115AG16GENIChomozygous108629371
1261350464261350465TC30GENIChomozygous109025997
1261350808261350809CT29GENIChomozygous109025998
1261350838261350839GT24GENIChomozygous109025999
1261351494261351495CT26GENIChomozygous120881347
1261354050261354051AC16GENIChomozygous109026001
1261354600261354601CT30GENIChomozygous109026002
1261354732261354733GA18GENIChomozygous109026003
1261355034261355035TC17GENIChomozygous109026007
1261355609261355610AC27GENIChomozygous109026008
1261355762261355763GA27GENIChomozygous109026009
1261355899261355900TC36GENIChomozygous108629382
1261355964261355965GT31GENIChomozygous109026010
1261356482261356483GA13GENIChomozygous109026011
1261356565261356566TC13GENIChomozygous108629385
1261356892261356893AG27GENIChomozygous108629386
1261357010261357011CT14GENIChomozygous109026012
1261357931261357932TC24GENIChomozygous108629387
1261358048261358049AC41GENIChomozygous108629388
1261358569261358570CT33GENIChomozygous109026013
1261358688261358689TG38GENIChomozygous109026014
1261359926261359927TC28GENIChomozygous108629391
1261361575261361576TA25GENIChomozygous109026018
1261361715261361716CT29GENIChomozygous109026019