| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:140664742-140664926 | Common:3; Rare:52 | ||||
| chr5:140691309-140691661 | Common:1; Rare:126; Clinvar:10; Clinvar (benign):2 | ||||
| chr5:141320228-141320550 | Common:2; Rare:73 | ||||
| chr5:141320611-141320864 | Common:2; Rare:66 | ||||
| chr5:141636808-141637001 | Common:2; Rare:84 | ||||
| chr5:141637323-141637459 | Common:1; Rare:33 | ||||
| chr5:141682191-141682395 | Common:2; Rare:57 | ||||
| chr5:141923750-141923910 | Common:1; Rare:44 | ||||
| chr5:141958179-141958364 | Rare:47 | ||||
| chr5:142012955-142013129 | Rare:54 | ||||
| chr5:142324152-142324326 | Rare:43 | ||||
| chr5:142324530-142324767 | Common:1; Rare:55 | ||||
| chr5:142324874-142325298 | Common:1; Rare:147 | ||||
| chr5:142644134-142644466 | Common:1; Rare:62 | ||||
| chr5:142698008-142698234 | Common:3; Rare:38 |