| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:105474129-105474394 | Common:2; Rare:118 | ||||
| chr14:105474565-105474955 | Common:3; Rare:287 | ||||
| chr14:105475031-105475309 | Rare:82 | ||||
| chr14:105475587-105476193 | Common:2; Rare:245 | ||||
| chr14:105486915-105487207 | Common:3; Rare:70 | ||||
| chr14:105489594-105489900 | Common:2; Rare:123 | ||||
| chr14:105489824-105490286 | Common:11; Rare:266 | ||||
| chr14:105490608-105491438 | Common:2; Rare:535 | ||||
| chr14:105491540-105491940 | Common:4; Rare:367 | ||||
| chr14:105525740-105526120 | Common:4; Rare:70 | ||||
| chr14:105526476-105526677 | Common:2; Rare:73 | ||||
| chr14:105528352-105528950 | Common:4; Rare:194 | ||||
| chr15:22785717-22786250 | Common:10; Rare:224 | ||||
| chr15:22786439-22786816 | Common:1; Rare:321; Clinvar:6; Clinvar (benign):6; Clinvar (pathogenic):2 | ||||
| chr15:22838353-22838818 | Common:8; Rare:392 |