Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr16:18801429-18801830 | Common:4; Rare:140; Clinvar:1 | ||||
chr16:19067394-19067685 | Common:5; Rare:105; Clinvar:1 | ||||
chr16:20806349-20806659 | Rare:100 | ||||
chr16:20900756-20900873 | Common:1; Rare:39 | ||||
chr16:21599390-21599757 | Common:4; Rare:126 | ||||
chr16:21953003-21953445 | Common:1; Rare:111; Clinvar (benign):3 | ||||
chr16:23453154-23453220 | Rare:19 | ||||
chr16:23557304-23557542 | Common:2; Rare:100; Clinvar:1; Clinvar (benign):2 | ||||
chr16:23641247-23641536 | Common:2; Rare:83; Clinvar:1; Clinvar (benign):3 | ||||
chr16:24729604-24729727 | Common:6; Rare:68 | ||||
chr16:25111472-25111843 | Common:2; Rare:106 | ||||
chr16:27268719-27268850 | Common:1; Rare:41 | ||||
chr16:27549877-27550167 | Common:2; Rare:111 | ||||
chr16:28538834-28539079 | Common:1; Rare:68 | ||||
chr16:28554170-28554343 | Common:2; Rare:61 |