| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:19192110-19192268 | Common:1; Rare:50 | ||||
| chr19:19192549-19192984 | Common:2; Rare:117 | ||||
| chr19:19516157-19516323 | Rare:100; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr19:19655213-19655338 | Rare:48 | ||||
| chr19:19659657-19659912 | Rare:87 | ||||
| chr19:19821692-19821875 | Common:1; Rare:60 | ||||
| chr19:29213131-29213295 | Common:3; Rare:54 | ||||
| chr19:29606027-29606320 | Common:2; Rare:88 | ||||
| chr19:29665253-29665471 | Common:4; Rare:79 | ||||
| chr19:29708609-29708921 | Common:2; Rare:61 | ||||
| chr19:29715046-29715305 | Common:1; Rare:96 | ||||
| chr19:32869698-32869894 | Common:2; Rare:38; Clinvar:1; Clinvar (benign):1 | ||||
| chr19:32971916-32972284 | Common:4; Rare:106 | ||||
| chr19:33081087-33081199 | Common:1; Rare:37 | ||||
| chr19:33373566-33373860 | Common:2; Rare:91 |