chr start stop reference nuc variant nuc depth genic status zygosity variant ID 8 55153521 55153522 C CTTTT 2 GENIC heterozygous 745699599 8 55155609 55155610 T - 7 GENIC homozygous 745699600 8 55156451 55156452 T G 22 GENIC possibly homozygous 631562572 8 55158014 55158015 T G 20 GENIC homozygous 631562573 8 55160016 55160017 C T 27 GENIC possibly homozygous 631562574 8 55160350 55160352 AT -- 16 GENIC possibly homozygous 745699602 8 55163678 55163679 A - 2 GENIC homozygous 745699603 8 55164338 55164339 C A 16 GENIC homozygous 631562575 8 55164385 55164386 G T 17 GENIC possibly homozygous 631562576 8 55165229 55165232 AAG --- 6 GENIC homozygous 745699604 8 55166695 55166696 A G 15 GENIC homozygous 631562577 8 55169644 55169645 T G 20 GENIC homozygous 631562578 8 55173247 55173248 A G 19 GENIC possibly homozygous 631562579 8 55173652 55173653 T C 26 GENIC possibly homozygous 631562580 8 55177790 55177791 T A 11 GENIC homozygous 631562581 8 55177795 55177796 C A 11 GENIC homozygous 631562582 8 55177796 55177797 C T 12 GENIC homozygous 631562583 8 55178721 55178722 A - 3 GENIC heterozygous 745699605 8 55179420 55179421 T C 23 GENIC homozygous 631562584 8 55180356 55180357 G A 22 GENIC homozygous 631562585 8 55180436 55180437 G C 9 GENIC homozygous 631562586 8 55181036 55181037 A AT 13 GENIC possibly homozygous 745699609 8 55182489 55182490 C CT 5 GENIC homozygous 745699610 8 55183473 55183474 G A 14 GENIC possibly homozygous 631562587 8 55186833 55186834 T - 1 GENIC homozygous 745699611 8 55187117 55187118 T C 12 GENIC homozygous 631562588 8 55193123 55193124 A G 22 GENIC homozygous 631562589 8 55193331 55193332 C T 27 GENIC homozygous 631562590 8 55193880 55193881 G A 19 GENIC heterozygous 631562591