| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:74019259-74019423 | Common:1; Rare:64 | ||||
| chr14:74084399-74084652 | Common:4; Rare:65 | ||||
| chr14:74348218-74348499 | Rare:63 | ||||
| chr14:74493406-74493770 | Common:4; Rare:119; Clinvar (benign):4 | ||||
| chr14:74713042-74713239 | Rare:110 | ||||
| chr14:74763231-74763399 | Rare:64 | ||||
| chr14:74881781-74881953 | Common:1; Rare:76 | ||||
| chr14:75002741-75002943 | Common:1; Rare:57; Clinvar:2 | ||||
| chr14:75127001-75127120 | Rare:38 | ||||
| chr14:75660797-75661334 | Common:4; Rare:128 | ||||
| chr14:76151765-76151962 | Rare:70 | ||||
| chr14:77320877-77321084 | Rare:59; Clinvar:1 | ||||
| chr14:77377045-77377415 | Common:2; Rare:109 | ||||
| chr14:77457536-77457884 | Common:1; Rare:104 | ||||
| chr14:77708000-77708124 | Rare:60 |