chr start stop reference nuc variant nuc depth genic status zygosity variant ID 4 58195798 58195799 C T 17 GENIC homozygous 112660583 4 58195864 58195865 G A 13 GENIC homozygous 112660585 4 58196430 58196431 C T 21 GENIC homozygous 112660587 4 58196951 58196952 C T 13 GENIC homozygous 112660589 4 58197361 58197362 A G 4 GENIC homozygous 112660591 4 58198281 58198282 G A 13 GENIC homozygous 112660593 4 58200033 58200034 C T 20 GENIC possibly homozygous 112660599 4 58201672 58201673 T C 32 GENIC homozygous 112660601 4 58202741 58202742 A G 17 GENIC homozygous 112660603 4 58203268 58203269 T C 16 GENIC homozygous 112660605 4 58203424 58203425 T C 13 GENIC homozygous 112660607 4 58203609 58203610 C T 23 GENIC homozygous 112660609 4 58204981 58204982 A G 13 GENIC homozygous 112660611 4 58205750 58205751 C T 19 GENIC homozygous 112660613 4 58205805 58205806 G A 19 GENIC homozygous 112660615 4 58205912 58205913 C A 31 GENIC homozygous 112660617 4 58206358 58206359 A G 28 GENIC homozygous 112660619 4 58206391 58206392 C T 30 GENIC homozygous 112660621 4 58208228 58208229 T C 30 GENIC homozygous 112660627 4 58207895 58207896 T C 20 GENIC homozygous 112660625 4 58208616 58208617 T C 28 GENIC homozygous 112660629 4 58211054 58211055 A G 14 GENIC homozygous 112660633 4 58211488 58211489 G A 19 GENIC homozygous 112660635 4 58211623 58211624 C T 20 GENIC homozygous 112660637 4 58211649 58211650 G T 21 GENIC homozygous 112660639 4 58214300 58214301 T C 8 GENIC homozygous 112660643 4 58215723 58215724 C G 26 GENIC homozygous 112660645 4 58216018 58216019 T C 20 GENIC homozygous 112660647 4 58211725 58211726 T C 17 GENIC homozygous 119276931