chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5141962530141962538GTGCGCGC68GENIChomozygous137346732
5141962725141962725A12GENIChomozygous146123772
5141962729141962729A13GENIChomozygous146123773
5141962726141962727GC12GENIChomozygous137641739
5141963013141963014CA43GENIChomozygous137641741
5141963323141963324GC49GENIChomozygous143965205
5141964051141964052CT57GENIChomozygous137641742
5141964207141964208GA49GENIChomozygous137641743
5141965628141965629CG29GENICheterozygous147665771
5141966688141966689TC46GENIChomozygous137641745
5141966708141966710TT45GENIChomozygous146123774
5141965636141965637TC31GENICheterozygous146143611
5141965648141965649GA32GENIChomozygous146143612
5141965889141965890GT44GENICpossibly homozygous146143613
5141966039141966040AG24GENIChomozygous146143614
5141967155141967156CG52GENICpossibly homozygous146143615
5141965668141965669AG31GENICheterozygous147866738
5141965670141965670CTCTTCTG30GENICheterozygous147866221
5141965675141965675CACGTGTACATGTATACAT27GENICheterozygous147866222