| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:5903831-5904135 | Common:6; Rare:106; Clinvar:5; Clinvar (benign):1 | ||||
| chr19:5978077-5978415 | Common:3; Rare:130 | ||||
| chr19:6110422-6110834 | Common:2; Rare:123 | ||||
| chr19:6393385-6393762 | Common:5; Rare:110 | ||||
| chr19:6684773-6685155 | Rare:100; Clinvar (benign):1 | ||||
| chr19:6710703-6711065 | Common:3; Rare:108; Clinvar:1; Clinvar (benign):2 | ||||
| chr19:6740627-6741125 | Common:1; Rare:128 | ||||
| chr19:7395033-7395185 | Common:4; Rare:47 | ||||
| chr19:7489006-7489103 | Rare:44 | ||||
| chr19:7535543-7535747 | Common:3; Rare:69; Clinvar:2 | ||||
| chr19:7629528-7629844 | Common:5; Rare:113; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr19:7637024-7637143 | Common:2; Rare:41; Clinvar (benign):1 | ||||
| chr19:7903542-7903929 | Rare:127 | ||||
| chr19:7920227-7920393 | Rare:74 | ||||
| chr19:7925523-7925759 | Common:2; Rare:64 |