| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:29606140-29606325 | Common:2; Rare:63 | ||||
| chr19:29665245-29665484 | Common:4; Rare:86 | ||||
| chr19:29714961-29715288 | Common:1; Rare:120; Clinvar:2; Clinvar (benign):1 | ||||
| chr19:29715514-29715677 | Rare:40 | ||||
| chr19:31349210-31349537 | Common:4; Rare:113 | ||||
| chr19:32405557-32405812 | Common:1; Rare:107 | ||||
| chr19:32438991-32439159 | Rare:37 | ||||
| chr19:32581031-32581326 | Common:4; Rare:113 | ||||
| chr19:32971843-32972321 | Common:5; Rare:140 | ||||
| chr19:33081126-33081221 | Common:1; Rare:39 | ||||
| chr19:33521747-33521972 | Common:1; Rare:75; Clinvar:5 | ||||
| chr19:34172363-34172718 | Common:1; Rare:129 | ||||
| chr19:34254324-34254606 | Rare:95 | ||||
| chr19:34365152-34365309 | Common:1; Rare:78 | ||||
| chr19:34428310-34428565 | Rare:88 |