| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:40750433-40750934 | Common:6; Rare:126 | ||||
| chr19:40751137-40751393 | Common:3; Rare:78 | ||||
| chr19:41218731-41218987 | Common:7; Rare:55 | ||||
| chr19:41219192-41219292 | Rare:21 | ||||
| chr19:41262307-41262580 | Rare:48 | ||||
| chr19:41310147-41310519 | Rare:133 | ||||
| chr19:41350762-41350961 | Common:1; Rare:41 | ||||
| chr19:41353856-41354172 | Common:1; Rare:91 | ||||
| chr19:41363767-41364005 | Common:1; Rare:82; Clinvar:1 | ||||
| chr19:41364123-41364229 | Rare:39; Clinvar:1 | ||||
| chr19:41397305-41397824 | Common:12; Rare:162; Clinvar (benign):4 | ||||
| chr19:41439525-41439674 | Common:1; Rare:44 | ||||
| chr19:41860043-41860666 | Common:6; Rare:220; Clinvar:4; Clinvar (benign):3 | ||||
| chr19:41898268-41898502 | Common:1; Rare:71 | ||||
| chr19:41906771-41906853 | Rare:28 |