| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:49155010-49155290 | Common:10; Rare:165 | ||||
| chr19:49155360-49155534 | Rare:31 | ||||
| chr19:49157643-49157871 | Common:1; Rare:134; Clinvar:2; Clinvar (benign):1 | ||||
| chr19:49361400-49361780 | Common:2; Rare:112 | ||||
| chr19:49451745-49451970 | Common:3; Rare:58 | ||||
| chr19:49453082-49453335 | Common:2; Rare:152 | ||||
| chr19:49453447-49453645 | Common:2; Rare:132 | ||||
| chr19:49478839-49479119 | Rare:165 | ||||
| chr19:49487278-49487662 | Common:10; Rare:252 | ||||
| chr19:49496062-49496501 | Common:4; Rare:293 | ||||
| chr19:49513109-49513474 | Common:2; Rare:156 | ||||
| chr19:49580517-49580712 | Common:1; Rare:99 | ||||
| chr19:49591077-49591231 | Common:4; Rare:49 | ||||
| chr19:49640080-49640560 | Common:1; Rare:234 | ||||
| chr19:49641770-49642258 | Rare:154 |