chr start stop reference nuc variant nuc depth genic status zygosity variant ID 7 99639111 99639112 T C 25 GENIC homozygous 799112575 7 99654233 99654234 G A 33 GENIC homozygous 799112576 7 99654291 99654292 G A 37 GENIC homozygous 799112577 7 99654401 99654402 T G 42 GENIC homozygous 799112578 7 99654485 99654486 C T 35 GENIC homozygous 799112579 7 99658862 99658863 T A 17 GENIC homozygous 799112580 7 99658926 99658927 A C 21 GENIC homozygous 799112581 7 99658948 99658949 A T 17 GENIC homozygous 799112582 7 99660024 99660025 A C 25 GENIC homozygous 799112583 7 99674307 99674308 C T 58 GENIC heterozygous 799112584 7 99674433 99674434 C T 65 GENIC heterozygous 799112585 7 99674472 99674473 C T 55 GENIC heterozygous 799112586 7 99674660 99674661 C A 58 GENIC heterozygous 799112587 7 99674778 99674779 C A 92 GENIC heterozygous 799112588 7 99674862 99674863 A C 100 GENIC heterozygous 799112589 7 99674890 99674891 G T 98 GENIC heterozygous 799112590 7 99674992 99674993 G A 90 GENIC heterozygous 799112591 7 99675082 99675083 G A 98 GENIC heterozygous 799112592 7 99675088 99675089 A C 98 GENIC heterozygous 799112593 7 99675096 99675097 C A 99 GENIC heterozygous 799112594 7 99675232 99675233 G C 103 GENIC heterozygous 799112595 7 99675277 99675278 C T 90 GENIC heterozygous 799112596 7 99675336 99675337 A G 67 GENIC heterozygous 799112597