| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:52447536-52448000 | Common:2; Rare:157 | ||||
| chr12:52449328-52449634 | Common:1; Rare:103 | ||||
| chr12:52450010-52450290 | Common:2; Rare:62 | ||||
| chr12:52487057-52487302 | Common:5; Rare:54 | ||||
| chr12:52488060-52488558 | Common:4; Rare:184; Clinvar:2; Clinvar (benign):1 | ||||
| chr12:52489162-52489545 | Common:9; Rare:81 | ||||
| chr12:52514407-52514717 | Common:9; Rare:54; Clinvar:1; Clinvar (benign):3 | ||||
| chr12:52522728-52522786 | Common:2; Rare:17 | ||||
| chr12:52806432-52806665 | Common:2; Rare:40 | ||||
| chr12:52807352-52807872 | Common:1; Rare:151; Clinvar:3; Clinvar (benign):2 | ||||
| chr12:52808292-52808859 | Common:4; Rare:167; Clinvar:3; Clinvar (benign):3 | ||||
| chr12:52846190-52846540 | Common:5; Rare:72 | ||||
| chr12:52867713-52867956 | Common:1; Rare:49 | ||||
| chr12:52874111-52874506 | Common:14; Rare:106 | ||||
| chr12:52876531-52876761 | Common:2; Rare:31 |