chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
185422790154227902AG51GENIChomozygous142654351
185422794654227947TG45GENIChomozygous142654352
185422805454228055GA49GENIChomozygous142654353
185422903854229039AG47GENIChomozygous142654354
185422915554229156TC51GENIChomozygous142654355
185422918554229186TC55GENIChomozygous142654356
185422928154229282GA37GENIChomozygous142654357
185422928754229288CG36GENIChomozygous142654358
185423023054230232CT51GENIChomozygous142631177
185423023854230239CA50GENIChomozygous142654359
185423036954230370AG42GENIChomozygous142654360
185423046254230463AC47GENIChomozygous142654361
185423143454231435GA33GENIChomozygous142654362
185423144154231442GC32GENIChomozygous142654363
185423154954231550AG42GENIChomozygous142654364
185423179954231800TC16GENICheterozygous142654365
185423186854231869GA22GENIChomozygous142654366
185423193554231936CT39GENIChomozygous142654367
185423195954231960CT43GENIChomozygous142654368
185423226154232262CT53GENIChomozygous142654369
185423244354232444AT48GENIChomozygous142654370
185423121354231213TA35GENIChomozygous142631178
185423180154231807ATTTAG15GENICheterozygous142631179
185423180854231812AATT14GENICheterozygous142631180
185423089654230897AC18GENICheterozygous403435176
185423089654230897A18GENIChomozygous403435177