chr start stop reference nuc variant nuc depth genic status zygosity variant ID 12 24750329 24750330 G T 18 GENIC possibly homozygous 50418608 12 24750403 24750404 G A 2 GENIC homozygous 50418610 12 24750475 24750476 G A 19 GENIC possibly homozygous 50418611 12 24750695 24750696 G A 19 GENIC homozygous 50418612 12 24750744 24750745 G A 19 GENIC possibly homozygous 50418613 12 24751490 24751494 CTCC ---- 4 GENIC homozygous 50418614 12 24751511 24751512 A G 7 GENIC homozygous 50418615 12 24751552 24751553 A G 18 GENIC homozygous 50418616 12 24751687 24751688 C T 11 GENIC possibly homozygous 50418617 12 24751713 24751714 G A 8 GENIC homozygous 50418618 12 24751740 24751741 G A 1 GENIC homozygous 50418619 12 24751827 24751828 G A 3 GENIC homozygous 50418622 12 24751874 24751875 A G 1 GENIC homozygous 50418623 12 24752338 24752340 AC -- 1 GENIC homozygous 50136204 12 24752525 24752526 G GT 1 GENIC homozygous 50136206 12 24753634 24753635 A G 9 GENIC possibly homozygous 50418629 12 24753887 24753888 T C 3 GENIC heterozygous 50418630 12 24754257 24754258 G A 22 GENIC possibly homozygous 50418631 12 24754858 24754862 AGGT ---- 7 GENIC homozygous 50418632 12 24755146 24755147 G A 20 GENIC possibly homozygous 50418634 12 24756036 24756037 A G 19 GENIC homozygous 50136214 12 24757349 24757350 C T 17 GENIC homozygous 50418637 12 24759895 24759896 A G 8 GENIC homozygous 50136218