chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7132339115132339116CG37GENIChomozygous143372303
7132339430132339431CT33GENIChomozygous138226972
7132340533132340534TC23GENIChomozygous143372304
7132341610132341611C13GENIChomozygous143352454
7132343314132343315TG31GENIChomozygous138226975
7132344415132344416TC21GENIChomozygous138226976
7132348089132348090AG27GENIChomozygous138226977
7132348406132348407AT23GENIChomozygous138226978
7132349607132349608TA25GENIChomozygous146461022
7132343492132343493CG16GENIChomozygous146461018
7132343990132343991GA19GENIChomozygous146461019
7132346660132346661GA18GENIChomozygous146461020
7132348959132348960CT30GENIChomozygous146461021
7132344285132344286G19GENIChomozygous146439177
7132349043132349043A25GENICpossibly homozygous146439178
7132345490132345490TTTGTTCTCGCAGTCGCCCTCTGGAGGTTAAGGTTGAGTACTGCTGTTTGGTGCAGGCCATTAATCTCAGGAAGCAGAGGCAGGCTGATC13GENIChomozygous137984568
7132350855132350856AG30GENIChomozygous138226979
7132350934132350935CT29GENIChomozygous146461023
7132352687132352688AG33GENIChomozygous146461024
7132353435132353436GA25GENICpossibly homozygous146461025
7132354044132354045AC25GENIChomozygous146461026
7132354282132354283TG29GENIChomozygous146461027
7132354627132354628TC28GENIChomozygous146461028
7132355315132355316AG28GENIChomozygous138226982
7132357392132357393G24GENICheterozygous403618484
7132357385132357386A25GENICheterozygous403227755
7132357385132357386AT25GENICpossibly homozygous403227756
7132357387132357388A25GENICheterozygous403618482
7132357387132357388AT25GENICpossibly homozygous403618483
7132357392132357393GA24GENICpossibly homozygous403618485
7132358295132358296CT26GENIChomozygous146461029
7132358469132358470CT18GENIChomozygous138226988
7132358767132358768GA9GENIChomozygous146461030