chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4143327156143327157GA7GENIChomozygous670454261
4143327733143327734GC8GENICpossibly homozygous670454262
4143327825143327826TC14GENIChomozygous670454263
4143327867143327868CT12GENIChomozygous670454264
4143328002143328110CCAGCCCTATCCTGAATTCCCTATGCCCATCAGGAAGGGTGGTCCTCGAGTGGCCCAGCCTTATCCTGAATTCTCCATGCCCATCAGCAAGGGTGGCCCTCGAGTACC------------------------------------------------------------------------------------------------------------9GENICheterozygous768742573
4143328147143328148GA12GENICheterozygous670454265
4143328775143328776AC13GENIChomozygous670454266
4143328931143328932CT15GENIChomozygous670454267
4143329836143329837GGATA1GENIChomozygous768742575
4143330688143330689TTGACA6GENICheterozygous768742577