| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:7516001-7516228 | Rare:52 | ||||
| chr19:7534054-7534187 | Common:3; Rare:35; Clinvar (benign):1 | ||||
| chr19:7629523-7629848 | Common:5; Rare:117; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr19:7637003-7637143 | Common:2; Rare:48; Clinvar (benign):1 | ||||
| chr19:7874300-7874512 | Common:1; Rare:53 | ||||
| chr19:7943644-7943988 | Rare:90 | ||||
| chr19:8005498-8005822 | Common:1; Rare:114 | ||||
| chr19:8308297-8308666 | Common:3; Rare:115 | ||||
| chr19:8321316-8321675 | Common:2; Rare:150 | ||||
| chr19:8363995-8364162 | Common:1; Rare:43 | ||||
| chr19:8390038-8390419 | Common:1; Rare:107 | ||||
| chr19:8444800-8445074 | Common:3; Rare:124 | ||||
| chr19:8514154-8514232 | Common:1; Rare:21 | ||||
| chr19:9140311-9140446 | Common:1; Rare:39 | ||||
| chr19:9323980-9324300 | Common:6; Rare:140 |