| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:2426639-2427049 | Common:3; Rare:157 | ||||
| chr19:2427436-2427716 | Common:3; Rare:132 | ||||
| chr19:2427827-2428003 | Common:4; Rare:73 | ||||
| chr19:2456668-2456790 | Common:1; Rare:30; Clinvar:1; Clinvar (benign):1 | ||||
| chr19:2456871-2457225 | Common:2; Rare:92; Clinvar:1; Clinvar (benign):1 | ||||
| chr19:2475837-2476259 | Common:3; Rare:140 | ||||
| chr19:2476584-2476659 | Rare:20 | ||||
| chr19:2721312-2721474 | Rare:39 | ||||
| chr19:2739941-2740231 | Rare:105 | ||||
| chr19:2783217-2783526 | Common:1; Rare:104 | ||||
| chr19:2785230-2785627 | Common:5; Rare:120 | ||||
| chr19:2819686-2820012 | Common:5; Rare:90 | ||||
| chr19:2841219-2841526 | Common:2; Rare:95 | ||||
| chr19:2900593-2901010 | Common:10; Rare:171 | ||||
| chr19:2944896-2945473 | Common:7; Rare:195 |