chr start stop reference nuc variant nuc depth genic status zygosity variant ID 18 60620465 60620466 T C 20 GENIC homozygous 951199251 18 60624918 60624919 A G 20 GENIC homozygous 951199252 18 60625800 60625801 T C 7 GENIC homozygous 951199253 18 60626632 60626633 T C 13 GENIC homozygous 951199254 18 60627484 60627485 T C 23 GENIC homozygous 951199255 18 60628219 60628220 G A 14 GENIC homozygous 951199256 18 60628292 60628293 G A 19 GENIC homozygous 951199257 18 60628800 60628801 A G 12 GENIC homozygous 951199258 18 60629052 60629053 C T 17 GENIC homozygous 951199259 18 60629248 60629249 G A 25 GENIC homozygous 951199260 18 60630749 60630750 A T 19 GENIC homozygous 951199261 18 60630945 60630946 C G 21 GENIC homozygous 951199262 18 60631097 60631098 C T 21 GENIC homozygous 951199263 18 60631478 60631479 C A 15 GENIC homozygous 951199264 18 60631670 60631671 A G 13 GENIC homozygous 951199265 18 60631920 60631921 G A 14 GENIC homozygous 951199266 18 60632136 60632137 C T 28 GENIC homozygous 951199267 18 60632157 60632158 G T 28 GENIC homozygous 951199268 18 60633066 60633067 T C 24 GENIC homozygous 951199269 18 60633665 60633666 G T 12 GENIC homozygous 951199270