| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:3434651-3435465 | Common:10; Rare:567 | ||||
| chr19:3477994-3478797 | Common:7; Rare:283 | ||||
| chr19:3479162-3480181 | Common:17; Rare:345 | ||||
| chr19:3500559-3501318 | Common:29; Rare:748 | ||||
| chr19:3505654-3506387 | Rare:718 | ||||
| chr19:3538893-3539293 | Common:3; Rare:138 | ||||
| chr19:3556843-3557874 | Common:36; Rare:1323 | ||||
| chr19:3572566-3573034 | Common:11; Rare:576 | ||||
| chr19:3573760-3574544 | Common:6; Rare:545 | ||||
| chr19:3576979-3577379 | Common:6; Rare:171 | ||||
| chr19:3585260-3586240 | Common:9; Rare:529; Clinvar:9; Clinvar (benign):24; Clinvar (pathogenic):3 | ||||
| chr19:3606170-3607108 | Common:2; Rare:602 | ||||
| chr19:3607248-3607725 | Common:2; Rare:181 | ||||
| chr19:3612640-3613220 | Common:16; Rare:495 | ||||
| chr19:3626044-3626767 | Common:5; Rare:226 |