| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:16324360-16325366 | Common:12; Rare:544 | ||||
| chr19:16471161-16471563 | Rare:142 | ||||
| chr19:16471867-16472291 | Common:25; Rare:478 | ||||
| chr19:16496019-16496477 | Common:14; Rare:724; Clinvar:6; Clinvar (benign):1 | ||||
| chr19:16542092-16542723 | Common:16; Rare:698 | ||||
| chr19:16571158-16571558 | Common:2; Rare:86 | ||||
| chr19:16571757-16572723 | Common:38; Rare:1128 | ||||
| chr19:16627893-16628949 | Common:12; Rare:1732 | ||||
| chr19:16628880-16629042 | Rare:44 | ||||
| chr19:16659630-16660452 | Common:29; Rare:1258 | ||||
| chr19:16660889-16661308 | Common:11; Rare:404 | ||||
| chr19:16829150-16829550 | Common:9; Rare:248 | ||||
| chr19:16887969-16888369 | Common:1; Rare:93 | ||||
| chr19:16888440-16889190 | Common:34; Rare:660 | ||||
| chr19:16889106-16889421 | Common:3; Rare:165 |