chr start stop reference nuc variant nuc depth genic status zygosity variant ID 19 34051573 34051574 G T 40 GENIC homozygous 145077475 19 34052416 34052416 TTT 60 GENIC homozygous 145068302 19 34052708 34052709 G A 45 GENIC homozygous 145077476 19 34052869 34052870 G T 57 GENIC homozygous 145077477 19 34054314 34054315 A 39 GENIC homozygous 145068303 19 34054330 34054330 A 39 GENIC possibly homozygous 145068304 19 34054710 34054711 G A 43 GENIC homozygous 145077478 19 34058033 34058036 TCT 14 GENIC homozygous 145068305 19 34059714 34059715 T C 41 GENIC homozygous 145077482 19 34056113 34056114 C A 53 GENIC homozygous 145077479 19 34056892 34056893 C T 63 GENIC homozygous 145077480 19 34057146 34057147 T C 34 GENIC homozygous 145077481 19 34060842 34060843 G A 46 GENIC homozygous 145077483 19 34061369 34061370 T C 49 GENIC homozygous 145077484 19 34061693 34061694 G A 42 GENIC homozygous 145077485 19 34062087 34062088 T C 57 GENIC homozygous 145077486 19 34062223 34062224 G A 46 GENIC homozygous 145077487 19 34062302 34062303 A G 52 GENIC homozygous 145077488 19 34063539 34063540 T C 53 GENIC homozygous 145077489 19 34063819 34063820 C T 58 GENIC homozygous 145077490 19 34064196 34064202 TTTGTT 28 GENIC homozygous 145068306 19 34064353 34064353 T 37 GENIC homozygous 145068307 19 34065143 34065144 T G 43 GENIC homozygous 145077491 19 34065449 34065450 C T 47 GENIC homozygous 145077492 19 34065575 34065576 T C 52 GENIC homozygous 145077493