chr start stop reference nuc variant nuc depth genic status zygosity variant ID 7 140571461 140571462 C CTTTT 17 GENIC possibly homozygous 749816984 7 140572424 140572425 G T 39 GENIC homozygous 638162315 7 140572685 140572688 TTT --- 27 GENIC possibly homozygous 749816985 7 140572686 140572688 TT -- 27 GENIC heterozygous 749816986 7 140572952 140572953 A G 33 GENIC homozygous 638162316 7 140573492 140573493 A G 36 GENIC homozygous 638162317 7 140574369 140574370 A G 21 GENIC homozygous 638162318 7 140574482 140574483 T C 45 GENIC homozygous 638162319 7 140574764 140574765 C T 28 GENIC homozygous 638162320 7 140576296 140576297 C CT 23 GENIC heterozygous 749816989 7 140576297 140576298 T - 23 GENIC heterozygous 749816988 7 140576502 140576503 G A 45 GENIC homozygous 638162321 7 140576874 140576875 A AT 34 GENIC possibly homozygous 749816990 7 140577113 140577114 A AG 4 GENIC heterozygous 749816991 7 140579414 140579415 T TCA 4 GENIC homozygous 749816992 7 140579436 140579437 G GAATAAATA 13 GENIC homozygous 749816995 7 140580004 140580005 A ACT 33 GENIC homozygous 749816996 7 140580850 140580851 A AGT 14 GENIC possibly homozygous 749816998 7 140580850 140580851 A AGTGT 14 GENIC heterozygous 749816999