chr start stop reference nuc variant nuc depth genic status zygosity variant ID 8 128028359 128028360 T C 23 GENIC homozygous 52884672 8 128028481 128028482 C CTTTTA 8 GENIC homozygous 52884673 8 128029653 128029654 C CTT 12 GENIC homozygous 52884674 8 128029661 128029662 T TTTG 13 GENIC homozygous 52884675 8 128029662 128029663 G GGTT 5 GENIC homozygous 52884677 8 128030090 128030091 T C 20 GENIC homozygous 52884678 8 128030446 128030447 T C 38 GENIC homozygous 52884679 8 128031132 128031133 G A 46 GENIC homozygous 52884680 8 128031353 128031354 C T 33 GENIC homozygous 52884681 8 128031364 128031365 C T 38 GENIC possibly homozygous 52884682 8 128032203 128032204 G A 44 GENIC homozygous 52884683 8 128032444 128032445 T C 36 GENIC homozygous 52884684 8 128032728 128032729 A ACAC 34 GENIC heterozygous 52884685 8 128033460 128033461 A G 34 GENIC homozygous 52884686 8 128033467 128033468 T A 34 GENIC homozygous 52884687 8 128034345 128034346 A AT 19 GENIC homozygous 52884688 8 128034693 128034695 CT -- 8 GENIC homozygous 52884689 8 128034695 128034701 CTTACC ------ 6 GENIC heterozygous 52884690 8 128034695 128034696 C - 6 GENIC heterozygous 52884691 8 128034696 128034699 TTA --- 6 GENIC homozygous 52884692 8 128034697 128034699 TA -- 6 GENIC homozygous 52884693 8 128035400 128035401 A AC 28 GENIC homozygous 52884694 8 128035410 128035411 C CA 30 GENIC homozygous 52884695 8 128035473 128035474 G A 33 GENIC homozygous 52884696 8 128035655 128035656 T TGG 15 GENIC homozygous 52884697