chr start stop reference nuc variant nuc depth genic status zygosity variant ID 16 49297877 49297878 G C 25 GENIC homozygous 962385201 16 49297880 49297881 C G 25 GENIC homozygous 962385202 16 49297901 49297902 C A 30 GENIC homozygous 962385203 16 49297949 49297950 G A 30 GENIC homozygous 962385204 16 49298498 49298499 C G 19 GENIC homozygous 962385205 16 49300595 49300596 G A 30 GENIC homozygous 962385206 16 49310356 49310357 A G 33 GENIC homozygous 962385207 16 49316984 49316985 G A 34 GENIC homozygous 962385208 16 49321001 49321002 T C 38 GENIC homozygous 962385209 16 49321341 49321342 T C 21 GENIC homozygous 962385210 16 49322929 49322930 C T 22 GENIC homozygous 962385211 16 49323114 49323115 G A 41 GENIC homozygous 962385212 16 49323222 49323223 A T 35 GENIC homozygous 962385213 16 49323305 49323306 C T 24 GENIC homozygous 962385214 16 49325269 49325270 T C 27 GENIC homozygous 962385215 16 49326197 49326198 T C 48 GENIC homozygous 962385216 16 49328078 49328079 T C 34 GENIC homozygous 962385217