| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:45667630-45668370 | Common:16; Rare:376 | ||||
| chr19:45668670-45668929 | Rare:78 | ||||
| chr19:45669375-45669775 | Common:2; Rare:110 | ||||
| chr19:45670280-45671150 | Common:1; Rare:215 | ||||
| chr19:45690992-45691392 | Rare:146 | ||||
| chr19:45691802-45692775 | Common:13; Rare:1138 | ||||
| chr19:45692828-45693228 | Common:2; Rare:79 | ||||
| chr19:45730778-45731233 | Common:6; Rare:417 | ||||
| chr19:45767643-45768990 | Common:6; Rare:1308; Clinvar:8; Clinvar (benign):21; Clinvar (pathogenic):5 | ||||
| chr19:45769179-45769801 | Common:15; Rare:1332 | ||||
| chr19:45770554-45770954 | Common:4; Rare:181; Clinvar:1 | ||||
| chr19:45771463-45771996 | Common:4; Rare:370; Clinvar (benign):2 | ||||
| chr19:45779446-45779901 | Common:7; Rare:456 | ||||
| chr19:45780299-45780714 | Common:4; Rare:174 | ||||
| chr19:45792265-45792665 | Rare:214 |