| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:39435846-39436169 | Common:7; Rare:119 | ||||
| chr19:39846310-39846473 | Common:1; Rare:77 | ||||
| chr19:39970969-39971238 | Common:2; Rare:73 | ||||
| chr19:39996932-39997101 | Common:5; Rare:54 | ||||
| chr19:40056157-40056260 | Rare:15 | ||||
| chr19:40090871-40090990 | Common:1; Rare:34 | ||||
| chr19:40279269-40279413 | Rare:25 | ||||
| chr19:40285233-40285462 | Common:1; Rare:80 | ||||
| chr19:40348388-40348739 | Common:4; Rare:117 | ||||
| chr19:40377873-40378041 | Common:2; Rare:71; Clinvar (benign):1 | ||||
| chr19:40425970-40426165 | Common:1; Rare:63 | ||||
| chr19:40444243-40444517 | Common:3; Rare:86 | ||||
| chr19:40576719-40576902 | Common:3; Rare:56 | ||||
| chr19:40715074-40715210 | Rare:37 | ||||
| chr19:40750411-40750582 | Common:3; Rare:55 |