| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:37172552-37172610 | Common:2; Rare:27 | ||||
| chr14:39114156-39114356 | Common:2; Rare:73 | ||||
| chr14:39174970-39175282 | Common:4; Rare:108 | ||||
| chr14:39267026-39267444 | Common:2; Rare:151 | ||||
| chr14:39432429-39432657 | Common:6; Rare:75 | ||||
| chr14:41606810-41607214 | Common:5; Rare:122 | ||||
| chr14:41607526-41607689 | Common:3; Rare:36 | ||||
| chr14:41607976-41608157 | Common:2; Rare:35 | ||||
| chr14:41608165-41608387 | Rare:52 | ||||
| chr14:44961897-44962279 | Common:3; Rare:110 | ||||
| chr14:45083943-45084185 | Common:1; Rare:93 | ||||
| chr14:45135683-45135979 | Common:1; Rare:58 | ||||
| chr14:45253084-45253310 | Rare:60 | ||||
| chr14:49586322-49586772 | Common:1; Rare:238; Clinvar (benign):1 | ||||
| chr14:49598675-49599023 | Common:2; Rare:136 |