| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:46788492-46788899 | Common:2; Rare:88 | ||||
| chr19:47113097-47113435 | Common:2; Rare:91 | ||||
| chr19:47256460-47256568 | Rare:39 | ||||
| chr19:47484163-47484318 | Common:2; Rare:50 | ||||
| chr19:48170243-48170704 | Common:2; Rare:128 | ||||
| chr19:48321345-48321502 | Common:1; Rare:46 | ||||
| chr19:48363913-48364037 | Common:2; Rare:44 | ||||
| chr19:48390887-48390996 | Rare:9 | ||||
| chr19:48391266-48391602 | Rare:102 | ||||
| chr19:48445659-48446025 | Common:4; Rare:127 | ||||
| chr19:48619139-48619435 | Rare:96 | ||||
| chr19:48872237-48872565 | Common:2; Rare:114 | ||||
| chr19:48965240-48965609 | Rare:115; Clinvar:3; Clinvar (benign):1; Clinvar (pathogenic):7 | ||||
| chr19:48993204-48993533 | Common:4; Rare:144; Clinvar:3; Clinvar (benign):3 | ||||
| chr19:48993553-48993912 | Common:5; Rare:94 |