chr start stop reference nuc variant nuc depth genic status zygosity variant ID 4 222553156 222553157 C CTT 20 GENIC homozygous 57103296 4 222553189 222553190 T C 35 GENIC homozygous 57103297 4 222553629 222553630 G - 35 GENIC homozygous 57103298 4 222553865 222553866 C T 32 GENIC possibly homozygous 57103299 4 222553908 222553909 C T 32 GENIC homozygous 57103300 4 222553988 222553989 T TAGA 27 GENIC homozygous 57103301 4 222554174 222554175 A AT 25 GENIC possibly homozygous 57103302 4 222554562 222554563 G GA 22 GENIC homozygous 57103303 4 222554717 222554718 C CT 23 GENIC homozygous 57103304 4 222554912 222554913 G A 46 GENIC homozygous 57103305 4 222555123 222555124 C T 46 GENIC homozygous 57103306 4 222556626 222556628 TT -- 18 GENIC heterozygous 57103307 4 222556642 222556643 G GTTC 24 GENIC heterozygous 57103308 4 222556902 222556903 T TTGTTTTG 18 GENIC possibly homozygous 57103310 4 222556946 222556947 C T 10 GENIC homozygous 57103311 4 222557127 222557128 A - 4 GENIC homozygous 57103312 4 222557261 222557262 T C 41 GENIC homozygous 57103313 4 222557760 222557761 T C 38 GENIC homozygous 57103314 4 222558307 222558308 T TA 40 GENIC homozygous 57103315 4 222559522 222559523 A ATT 24 GENIC homozygous 57103316 4 222559746 222559752 TTTTGT ------ 17 GENIC homozygous 57103317 4 222560144 222560145 C CT 13 GENIC heterozygous 57103318