| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:35046141-35046529 | Common:1; Rare:131 | ||||
| chr14:35122244-35122806 | Common:2; Rare:156 | ||||
| chr14:35402808-35403154 | Common:4; Rare:102; Clinvar (benign):4 | ||||
| chr14:35404516-35404804 | Common:3; Rare:104; Clinvar:1; Clinvar (benign):4 | ||||
| chr14:37197874-37198116 | Common:2; Rare:73 | ||||
| chr14:37595328-37595678 | Common:1; Rare:96 | ||||
| chr14:37595998-37596058 | Common:1; Rare:7 | ||||
| chr14:39114137-39114341 | Common:2; Rare:65 | ||||
| chr14:39174997-39175282 | Common:3; Rare:98 | ||||
| chr14:39432431-39432618 | Common:6; Rare:60 | ||||
| chr14:44961892-44962239 | Common:3; Rare:100 | ||||
| chr14:45135723-45135979 | Common:1; Rare:48 | ||||
| chr14:45253067-45253312 | Rare:67 | ||||
| chr14:45253475-45253632 | Common:2; Rare:69 | ||||
| chr14:49586327-49586772 | Common:1; Rare:237; Clinvar (benign):1 |