chr start stop reference nuc variant nuc depth genic status zygosity variant ID 18 60619492 60619493 A G 8 GENIC homozygous 977510567 18 60620465 60620466 T C 22 GENIC homozygous 977510568 18 60620560 60620561 G T 18 GENIC homozygous 977510569 18 60620603 60620604 T C 16 GENIC homozygous 977510570 18 60625800 60625801 T C 11 GENIC homozygous 977510571 18 60626632 60626633 T C 34 GENIC homozygous 977510572 18 60627484 60627485 T C 20 GENIC homozygous 977510573 18 60628219 60628220 G A 23 GENIC homozygous 977510574 18 60628800 60628801 A G 19 GENIC homozygous 977510575 18 60629023 60629024 T C 20 GENIC homozygous 977510576 18 60629052 60629053 C T 17 GENIC possibly homozygous 977510577 18 60629248 60629249 G A 27 GENIC homozygous 977510578 18 60630749 60630750 A T 21 GENIC homozygous 977510579 18 60630945 60630946 C G 18 GENIC homozygous 977510580 18 60631097 60631098 C T 29 GENIC homozygous 977510581 18 60631478 60631479 C A 26 GENIC homozygous 977510582 18 60631670 60631671 A G 23 GENIC homozygous 977510583 18 60632136 60632137 C T 23 GENIC homozygous 977510584 18 60632157 60632158 G T 27 GENIC homozygous 977510585 18 60633066 60633067 T C 30 GENIC homozygous 977510586 18 60633665 60633666 G T 11 GENIC possibly homozygous 977510587