| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:28766547-28766791 | Common:2; Rare:73 | ||||
| chr14:32203245-32203673 | Common:13; Rare:188 | ||||
| chr14:41604865-41604993 | Common:2; Rare:24 | ||||
| chr14:41605286-41605376 | Common:2; Rare:15 | ||||
| chr14:41605414-41605473 | Common:1; Rare:15 | ||||
| chr14:49633956-49634064 | Common:1; Rare:43; Clinvar:3; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr14:49862639-49862864 | Common:1; Rare:119 | ||||
| chr14:51094241-51094576 | Rare:68 | ||||
| chr14:56812964-56813341 | Common:3; Rare:75 | ||||
| chr14:58271419-58271482 | Rare:18 | ||||
| chr14:59325807-59326077 | Common:1; Rare:36 | ||||
| chr14:62117248-62117519 | Common:2; Rare:51 | ||||
| chr14:68628379-68628426 | Common:1; Rare:13 | ||||
| chr14:68795244-68795425 | Common:3; Rare:40 | ||||
| chr14:69886137-69886284 | Rare:15 |