| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:67935647-67935972 | Common:1; Rare:111 | ||||
| chr16:67944240-67944640 | Rare:120 | ||||
| chr16:67966639-67967600 | Common:2; Rare:280 | ||||
| chr16:67968540-67968880 | Common:2; Rare:114 | ||||
| chr16:68023195-68023347 | Common:1; Rare:46 | ||||
| chr16:68084571-68084853 | Rare:51 | ||||
| chr16:68084965-68085455 | Common:3; Rare:110 | ||||
| chr16:68237535-68237893 | Rare:98 | ||||
| chr16:68245148-68245420 | Common:1; Rare:80 | ||||
| chr16:68264270-68264770 | Common:1; Rare:138 | ||||
| chr16:68310881-68311159 | Common:3; Rare:130 | ||||
| chr16:68448541-68448853 | Common:1; Rare:73 | ||||
| chr16:68529920-68530190 | Common:6; Rare:132 | ||||
| chr16:68539138-68539382 | Common:2; Rare:111 | ||||
| chr16:68644940-68646192 | Common:9; Rare:603; Clinvar:15; Clinvar (benign):1 |