chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X7835986178359862CT14GENIChomozygous108392420
X7836344478363445TG8GENIChomozygous108392422
X7836566978365670GC8GENIChomozygous108276464
X7836854578368546GA4GENIChomozygous108392424
X7837034578370346TC21GENICheterozygous108276466
X7837036278370363TC21GENICheterozygous108276468
X7837037078370371AG20GENICheterozygous108276470
X7837047078370471TG13GENICheterozygous108732917
X7837191278371913GA9GENIChomozygous108392426
X7837615578376156AT9GENIChomozygous108392428
X7837670778376708GT16GENIChomozygous108276472
X7837942378379424TC16GENIChomozygous108276474
X7838178178381782GA4GENIChomozygous108276476
X7839145478391455GA13GENICpossibly homozygous108392430
X7839316878393169TA10GENIChomozygous108392432
X7839458578394586TC2GENIChomozygous108551522
X7839458778394588TC2GENIChomozygous108732919
X7839696678396967AG29GENIChomozygous108392434
X7839865278398653CA7GENIChomozygous108392436
X7838899478388995TC3GENIChomozygous108596578