| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:24242543-24243166 | Common:3; Rare:142; Clinvar:1; Clinvar (benign):3 | ||||
| chr14:24270949-24271341 | Common:4; Rare:112 | ||||
| chr14:24271435-24271831 | Common:2; Rare:104 | ||||
| chr14:24299671-24299933 | Common:5; Rare:88 | ||||
| chr14:24300098-24300175 | Common:1; Rare:28 | ||||
| chr14:24310700-24310859 | Common:1; Rare:69 | ||||
| chr14:24311403-24311529 | Common:2; Rare:59 | ||||
| chr14:24339390-24339498 | Rare:34 | ||||
| chr14:24339904-24340144 | Common:2; Rare:54 | ||||
| chr14:24365744-24365934 | Common:3; Rare:37 | ||||
| chr14:24366639-24366905 | Common:1; Rare:70 | ||||
| chr14:24367353-24367380 | Rare:11 | ||||
| chr14:24367635-24367682 | Rare:12 | ||||
| chr14:24367831-24367962 | Rare:24 | ||||
| chr14:24368679-24368762 | Rare:18 |