| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:44747892-44748094 | Common:1; Rare:38 | ||||
| chr19:44757412-44757723 | Common:1; Rare:66 | ||||
| chr19:44777720-44778031 | Rare:101 | ||||
| chr19:44955251-44955430 | Common:2; Rare:57 | ||||
| chr19:45079161-45079297 | Rare:36 | ||||
| chr19:45091600-45091777 | Common:1; Rare:47 | ||||
| chr19:45370552-45370731 | Common:2; Rare:52 | ||||
| chr19:45405006-45405163 | Rare:34 | ||||
| chr19:45406290-45406687 | Common:2; Rare:96 | ||||
| chr19:45423480-45423813 | Common:3; Rare:69; Clinvar (benign):1 | ||||
| chr19:45450733-45450984 | Common:4; Rare:46 | ||||
| chr19:45507228-45507528 | Common:1; Rare:83 | ||||
| chr19:45522161-45522462 | Rare:104 | ||||
| chr19:45692538-45692713 | Rare:42 | ||||
| chr19:45730860-45731058 | Common:1; Rare:41 |