| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:49633956-49634079 | Common:1; Rare:49; Clinvar:6; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr14:49862642-49863007 | Common:1; Rare:169 | ||||
| chr14:62117297-62117494 | Common:2; Rare:37 | ||||
| chr14:69886145-69886376 | Rare:27 | ||||
| chr14:75981867-75982073 | Common:2; Rare:47 | ||||
| chr14:81170391-81170489 | Rare:27 | ||||
| chr14:81219339-81219525 | Rare:41 | ||||
| chr14:96039196-96039380 | Common:2; Rare:51 | ||||
| chr14:100825944-100826169 | Rare:48 | ||||
| chr14:100829093-100829324 | Common:1; Rare:36 | ||||
| chr15:22494645-22494898 | Common:1; Rare:32 | ||||
| chr15:23303465-23303775 | Rare:25 | ||||
| chr15:28589238-28589505 | Common:1; Rare:9 | ||||
| chr15:37102005-37102259 | Common:1; Rare:62 | ||||
| chr15:39580208-39580431 | Common:1; Rare:55 |