| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:39203878-39203921 | Common:1; Rare:4 | ||||
| chr14:39204026-39204299 | Common:3; Rare:50 | ||||
| chr14:39228691-39228723 | Rare:4 | ||||
| chr14:44962743-44962838 | Rare:25 | ||||
| chr14:45212365-45212528 | Common:4; Rare:30 | ||||
| chr14:46445775-46445880 | Rare:27 | ||||
| chr14:48963358-48963507 | Rare:29 | ||||
| chr14:49106797-49106976 | Common:3; Rare:47 | ||||
| chr14:49505440-49505753 | Common:2; Rare:46 | ||||
| chr14:49599728-49599894 | Common:3; Rare:48 | ||||
| chr14:49621443-49621684 | Common:2; Rare:92; Clinvar:1; Clinvar (benign):2 | ||||
| chr14:49633779-49634142 | Common:2; Rare:141; Clinvar:13; Clinvar (benign):7; Clinvar (pathogenic):2 | ||||
| chr14:49634205-49634532 | Common:1; Rare:153; Clinvar:9; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr14:49641747-49641969 | Common:2; Rare:57 | ||||
| chr14:49687352-49687640 | Rare:61 |