| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:73591976-73592204 | Common:2; Rare:94 | ||||
| chr14:73644730-73645084 | Common:3; Rare:99; Clinvar:2; Clinvar (benign):1 | ||||
| chr14:73713812-73714031 | Rare:61 | ||||
| chr14:73714307-73714682 | Common:3; Rare:113 | ||||
| chr14:73760174-73760566 | Common:3; Rare:78 | ||||
| chr14:73760613-73760723 | Common:1; Rare:25 | ||||
| chr14:73786670-73786927 | Common:1; Rare:60 | ||||
| chr14:73787093-73787478 | Common:4; Rare:121 | ||||
| chr14:73787712-73787955 | Common:3; Rare:39 | ||||
| chr14:73851724-73852109 | Common:8; Rare:114 | ||||
| chr14:73886504-73887009 | Common:4; Rare:146 | ||||
| chr14:73950053-73950370 | Common:6; Rare:147; Clinvar (benign):4 | ||||
| chr14:73950486-73950637 | Common:1; Rare:40; Clinvar (benign):1 | ||||
| chr14:74018596-74018783 | Common:2; Rare:38 | ||||
| chr14:74018940-74019429 | Common:4; Rare:147 |