| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:103333833-103334454 | Common:6; Rare:230 | ||||
| chr14:103334616-103334906 | Common:2; Rare:128 | ||||
| chr14:103334962-103335089 | Rare:48 | ||||
| chr14:103335136-103335170 | Rare:5 | ||||
| chr14:103335443-103335731 | Common:1; Rare:75 | ||||
| chr14:103385197-103385546 | Common:1; Rare:122 | ||||
| chr14:103521679-103521751 | Common:1; Rare:21 | ||||
| chr14:103522134-103522434 | Rare:114 | ||||
| chr14:103522738-103522995 | Rare:87 | ||||
| chr14:103528971-103529297 | Common:1; Rare:86 | ||||
| chr14:103561368-103561645 | Common:1; Rare:58 | ||||
| chr14:103562227-103562486 | Common:1; Rare:108 | ||||
| chr14:103562559-103563326 | Common:11; Rare:314; Clinvar:1; Clinvar (benign):9 | ||||
| chr14:103628710-103628797 | Rare:21 | ||||
| chr14:103628828-103629265 | Common:3; Rare:138 |