| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:100568066-100568392 | Common:9; Rare:125 | ||||
| chr14:100568449-100568890 | Common:2; Rare:163 | ||||
| chr14:100568943-100569049 | Rare:24 | ||||
| chr14:100586680-100587260 | Common:8; Rare:221 | ||||
| chr14:100587250-100587700 | Common:15; Rare:248 | ||||
| chr14:101561051-101561551 | Common:3; Rare:221 | ||||
| chr14:101761370-101761830 | Common:15; Rare:225 | ||||
| chr14:101809634-101809893 | Rare:85 | ||||
| chr14:101810190-101810530 | Common:2; Rare:90 | ||||
| chr14:101964193-101964644 | Common:7; Rare:198; Clinvar:2; Clinvar (benign):1 | ||||
| chr14:102087008-102087346 | Common:8; Rare:265 | ||||
| chr14:102087400-102087690 | Common:3; Rare:117 | ||||
| chr14:102139120-102139490 | Rare:202 | ||||
| chr14:102139654-102139936 | Rare:184 | ||||
| chr14:102305124-102305284 | Common:2; Rare:94 |