chr start stop reference nuc variant nuc depth genic status zygosity variant ID 10 62691992 62691993 G A 17 GENIC homozygous 116614115 10 62692104 62692105 A G 11 GENIC homozygous 116614117 10 62692804 62692805 C T 21 GENIC homozygous 116614121 10 62693532 62693532 GA 11 GENIC homozygous 128823494 10 62694135 62694136 T C 14 GENIC homozygous 116614123 10 62694971 62694972 T A 23 GENIC homozygous 116614125 10 62694989 62694990 T C 18 GENIC homozygous 116614127 10 62695670 62695671 G 12 GENIC homozygous 128823495 10 62696391 62696392 C T 27 GENIC homozygous 116614129 10 62696808 62696808 TGTGTGTGTG 8 GENIC homozygous 128823496 10 62697204 62697205 T G 21 GENIC homozygous 116614131 10 62697810 62697811 A C 20 GENIC homozygous 116614133 10 62697853 62697854 T C 19 GENIC homozygous 116614135 10 62697955 62697956 C G 13 GENIC homozygous 116614137 10 62697961 62697962 C G 12 GENIC homozygous 118084062 10 62698680 62698680 AGG 14 GENIC homozygous 128823497 10 62696887 62696888 G A 10 GENIC homozygous 117997700 10 62698392 62698393 G A 16 GENIC homozygous 116614139 10 62699211 62699212 A G 11 GENIC homozygous 116614141