chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
10100806773100806774A45GENIChomozygous143436372
10100807469100807479TTTTTTTTTG37GENICpossibly homozygous143436373
10100808474100808475GC34GENIChomozygous143468393
10100808603100808604CG30GENIChomozygous143468394
10100808604100808605TC32GENIChomozygous143468395
10100809658100809659AC43GENICpossibly homozygous143468396
10100810170100810171GA48GENIChomozygous143468397
10100810816100810817TG18GENIChomozygous143468398
10100812213100812213T7GENICheterozygous144079726
10100812216100812217CT20GENIChomozygous143468399
10100813872100813873AG64GENIChomozygous143468400
10100814741100814742AG62GENIChomozygous143468401
10100814995100815080GCCAGCACTGTACGTACCAACCTTTGGTTTTTTTTTTTTTTTTTTTTGGTTCTTTTTTTTTTCGGAGCTGGGGACCGAACCCAGG35GENIChomozygous143436374
10100815132100815132T31GENIChomozygous143436375
10100816005100816017TTTTTTTTTTTC16GENICpossibly homozygous144079728
10100816115100816116TC40GENIChomozygous143468402
10100819393100819415GTGTGTGTGTGTGCGTGCGTGC46GENIChomozygous143436376
10100819484100819485GA58GENIChomozygous143468403
10100819990100819991AG55GENIChomozygous143468404
10100820484100820485AC45GENIChomozygous143468405
10100820660100820660CCTC52GENIChomozygous143436377
10100824726100824727CA50GENICpossibly homozygous143468406
10100813028100813029AG36GENIChomozygous142265711
10100819412100819413TC46GENICheterozygous154664447
10100819412100819413T46GENIChomozygous404017398