chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
32170632321706323G29GENIChomozygous127859506
32171017421710175T39GENICheterozygous127859507
32172359921723600TG35GENICheterozygous111504302
32174614821746149G34GENIChomozygous127859515
32174615421746154T34GENIChomozygous127859516
32174619321746194CT32GENIChomozygous111504330
32174619621746197G31GENIChomozygous127859517
32174621421746214C29GENIChomozygous127859518
32174749821747499CA35GENIChomozygous111504331
32174750421747505A34GENIChomozygous127859519
32174751021747511GC34GENIChomozygous111504333
32174753221747533CA36GENIChomozygous111504335
32174755121747553TG35GENIChomozygous127859520
32174771621747716T1GENIChomozygous127859521
32174792821747929A6GENIChomozygous127859522
32174804721748047G18GENICpossibly homozygous127859523
32174812321748124G20GENIChomozygous127859524
32174816621748167G31GENIChomozygous127859525
32176841921768419TGGGG20GENIChomozygous127859528
32176842021768420TTTAGCTCAGTGGTAGAGCGCTTGCCTAGC20GENIChomozygous127859529
32176842321768424GA27GENIChomozygous121755751
32180098721800988CG37GENICheterozygous130644811
32174760921747610G17GENIChomozygous129888256
32180096721800968CG37GENICheterozygous130644810