chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
183942803239428033CT20GENIChomozygous110328221
183942919039429191GA22GENIChomozygous110328223
183942962939429630TA35GENIChomozygous110328225
183943175039431751TC31GENIChomozygous110328227
183943338339433384CT27GENIChomozygous110328229
183943458539434586CA22GENICpossibly homozygous110328231
183943621639436217CG22GENIChomozygous110328233
183943632339436324GA27GENIChomozygous110328235
183943723139437232TC21GENIChomozygous110328237
183943773339437734CA30GENIChomozygous110463273
183943773439437735AC31GENIChomozygous110463274
183943799939438000TC9GENIChomozygous110463275
183943800039438001CT9GENIChomozygous110463276
183943968739439688TC21GENIChomozygous110328241
183944184139441842CT34GENIChomozygous110328243
183944264939442650TG22GENIChomozygous110328245
183944514939445150TA26GENIChomozygous110328247
183944569539445696AC27GENIChomozygous110328249
183944614839446149CT29GENIChomozygous110328251
183944688939446890AG22GENIChomozygous110328253
183944773239447733GA28GENIChomozygous110328255
183944939039449391GA38GENIChomozygous110328257
183945053739450538CT28GENIChomozygous110328259
183945099539450996TC39GENIChomozygous110328261
183945306039453061CT27GENIChomozygous110328263
183945398439453985CA17GENIChomozygous110328265
183945683739456838TA31GENIChomozygous110328267
183945692439456925GA24GENIChomozygous110328269
183945736839457369GA34GENIChomozygous110328271
183946099239460993CG37GENIChomozygous110328273
183946323939463240TC23GENIChomozygous110328275
183946738639467387CT27GENIChomozygous110328277
183946835739468358AG31GENIChomozygous110328279
183946857539468576AG31GENIChomozygous110328281
183946939439469395TC26GENIChomozygous110328283
183947500439475005GT29GENIChomozygous110328285
183947548439475485GA29GENIChomozygous110328287