chr start stop reference nuc variant nuc depth genic status zygosity variant ID 8 59594124 59594125 C A 24 GENIC homozygous 53272590 8 59594533 59594534 C T 22 GENIC homozygous 53272591 8 59595061 59595062 T C 34 GENIC homozygous 52664068 8 59595243 59595244 T C 18 GENIC homozygous 53272592 8 59596324 59596325 G A 30 GENIC possibly homozygous 53272593 8 59596559 59596560 T C 21 GENIC homozygous 53272594 8 59596834 59596835 T TG 2 GENIC homozygous 52664074 8 59596884 59596885 C A 8 GENIC homozygous 52664076 8 59597237 59597238 C T 9 GENIC homozygous 53272595 8 59597256 59597257 G A 11 GENIC heterozygous 53272596 8 59597256 59597257 G GTGTAA 9 GENIC homozygous 53272597 8 59597365 59597366 C A 11 GENIC homozygous 53272598 8 59597392 59597393 G A 7 GENIC homozygous 53272599 8 59597430 59597431 C CAAA 15 GENIC possibly homozygous 52983291 8 59596887 59596889 AA -- 5 GENIC heterozygous 52983289 8 59597470 59597471 C T 22 GENIC homozygous 53272600 8 59597687 59597688 G A 15 GENIC homozygous 53272601 8 59598668 59598669 A - 19 GENIC homozygous 52983292 8 59599276 59599277 C T 24 GENIC homozygous 53272602 8 59599291 59599292 C T 25 GENIC homozygous 53272603 8 59602402 59602403 T TA 25 GENIC homozygous 53272604 8 59602616 59602617 T A 47 GENIC homozygous 53272605 8 59604055 59604056 G A 22 GENIC homozygous 53272606 8 59604494 59604495 C A 11 GENIC homozygous 53272607 8 59604655 59604656 C T 19 GENIC homozygous 53272608 8 59605092 59605093 T - 1 GENIC homozygous 52664090 8 59603281 59603282 A G 21 GENIC homozygous 52664084 8 59603988 59603989 T C 24 GENIC homozygous 52664086 8 59604977 59604978 A - 4 GENIC homozygous 52664088 8 59605328 59605329 C A 19 GENIC possibly homozygous 53272609 8 59605333 59605334 A AC 21 GENIC homozygous 53122433 8 59606721 59606722 G T 19 GENIC homozygous 53272610