| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:92882412-92882732 | Common:2; Rare:99 | ||||
| chr15:93000455-93000587 | Rare:40; Clinvar:2; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr15:96327340-96327441 | Common:3; Rare:15 | ||||
| chr15:99105809-99105888 | Rare:34 | ||||
| chr16:399442-399738 | Common:4; Rare:104 | ||||
| chr16:519510-519805 | Common:2; Rare:81 | ||||
| chr16:2123496-2123543 | Rare:20 | ||||
| chr16:2603103-2603493 | Common:3; Rare:152 | ||||
| chr16:2673317-2673706 | Common:10; Rare:141 | ||||
| chr16:3022914-3023239 | Rare:89 | ||||
| chr16:3026658-3026908 | Common:1; Rare:98; Clinvar (pathogenic):1 | ||||
| chr16:3152682-3152920 | Common:3; Rare:107 | ||||
| chr16:4335205-4335294 | Rare:33 | ||||
| chr16:8815430-8815571 | Common:2; Rare:38 | ||||
| chr16:8847534-8847859 | Common:1; Rare:139; Clinvar:9; Clinvar (benign):6; Clinvar (pathogenic):8 |