chr start stop reference nuc variant nuc depth genic status zygosity variant ID 2 206548995 206548996 C CT 26 GENIC homozygous 683603957 2 206551492 206551493 C T 62 GENIC homozygous 504978213 2 206552309 206552310 A C 53 GENIC homozygous 503226618 2 206552411 206552423 CGCACGCACACA ------------ 11 GENIC homozygous 683603960 2 206553148 206553149 G A 36 GENIC homozygous 503226619 2 206553905 206553906 A G 58 GENIC homozygous 503226620 2 206554619 206554620 A G 25 GENIC homozygous 503226621 2 206555172 206555173 T C 54 GENIC homozygous 503226622 2 206555328 206555329 T C 40 GENIC homozygous 503226623 2 206555423 206555424 A C 29 GENIC heterozygous 504978214 2 206555701 206555702 A G 18 GENIC heterozygous 503226624 2 206555705 206555706 A G 17 GENIC heterozygous 504978215 2 206555728 206555729 G A 20 GENIC possibly homozygous 504978216 2 206556318 206556319 A ACC 23 GENIC possibly homozygous 683603961 2 206556318 206556319 A AC 23 GENIC heterozygous 683603962 2 206556565 206556566 G A 45 GENIC homozygous 503226625 2 206556797 206556798 C A 50 GENIC homozygous 504978217 2 206557459 206557460 A G 44 GENIC homozygous 503226626 2 206558002 206558003 T C 30 GENIC homozygous 503226627 2 206558112 206558113 T C 48 GENIC homozygous 503226628 2 206558569 206558570 G C 38 GENIC homozygous 504978218 2 206558597 206558598 G A 41 GENIC homozygous 504978219 2 206559182 206559183 A G 54 GENIC homozygous 503226629 2 206559625 206559626 A C 37 GENIC possibly homozygous 504978220 2 206559823 206559824 C T 33 GENIC possibly homozygous 504978221 2 206560906 206560907 G A 50 GENIC heterozygous 503226630 2 206561062 206561063 T C 47 GENIC homozygous 503226631 2 206562831 206562832 T TCACA 9 GENIC heterozygous 683603963 2 206562831 206562832 T TCA 9 GENIC heterozygous 683603965 2 206562832 206562834 CA -- 9 GENIC heterozygous 683603964