| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:49598731-49599023 | Common:1; Rare:107 | ||||
| chr14:49620563-49620820 | Common:2; Rare:103; Clinvar:1 | ||||
| chr14:50312207-50312374 | Rare:64 | ||||
| chr14:50396863-50396987 | Common:1; Rare:32 | ||||
| chr14:50561124-50561206 | Rare:15 | ||||
| chr14:50668327-50668556 | Common:3; Rare:85 | ||||
| chr14:50944379-50944595 | Common:4; Rare:78; Clinvar:1; Clinvar (benign):2 | ||||
| chr14:51240081-51240305 | Common:1; Rare:91 | ||||
| chr14:51488918-51489147 | Common:1; Rare:40 | ||||
| chr14:51651666-51651968 | Common:4; Rare:84 | ||||
| chr14:51989396-51989647 | Common:2; Rare:87 | ||||
| chr14:52004107-52004236 | Common:1; Rare:50 | ||||
| chr14:52707074-52707226 | Common:1; Rare:64 | ||||
| chr14:52791447-52791792 | Common:2; Rare:118 | ||||
| chr14:52951161-52951443 | Common:3; Rare:117 |