| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:49189434-49189487 | Rare:9 | ||||
| chr19:49369824-49369967 | Common:2; Rare:34 | ||||
| chr19:49408833-49409030 | Common:2; Rare:46 | ||||
| chr19:49689557-49689598 | Rare:14 | ||||
| chr19:49745281-49745549 | Common:3; Rare:74 | ||||
| chr19:49781757-49782033 | Rare:63 | ||||
| chr19:49828735-49829087 | Rare:94; Clinvar:1; Clinvar (benign):1 | ||||
| chr19:49829856-49830187 | Common:1; Rare:123; Clinvar:7; Clinvar (benign):4 | ||||
| chr19:49832232-49832373 | Common:3; Rare:38; Clinvar:2; Clinvar (benign):1 | ||||
| chr19:49849797-49849982 | Common:1; Rare:31 | ||||
| chr19:50266995-50267131 | Common:1; Rare:31 | ||||
| chr19:50319571-50319806 | Common:4; Rare:55 | ||||
| chr19:50334208-50334362 | Common:1; Rare:52 | ||||
| chr19:50604234-50604364 | Common:4; Rare:26 | ||||
| chr19:50604733-50604965 | Common:13; Rare:36 |