| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:11435157-11435694 | Common:7; Rare:163; Clinvar:2; Clinvar (benign):5 | ||||
| chr19:11529077-11529289 | Rare:41 | ||||
| chr19:11539803-11540015 | Rare:44 | ||||
| chr19:11559192-11559407 | Common:1; Rare:68 | ||||
| chr19:11738869-11739255 | Common:4; Rare:101 | ||||
| chr19:11766889-11767175 | Common:1; Rare:73 | ||||
| chr19:11887668-11887857 | Common:1; Rare:59 | ||||
| chr19:11924961-11925138 | Common:6; Rare:48 | ||||
| chr19:11964910-11965082 | Common:1; Rare:44 | ||||
| chr19:12140335-12140609 | Rare:67 | ||||
| chr19:12156665-12156855 | Common:1; Rare:45 | ||||
| chr19:12162991-12163127 | Rare:48 | ||||
| chr19:12294748-12295059 | Common:1; Rare:84 | ||||
| chr19:12365608-12365809 | Common:3; Rare:53 | ||||
| chr19:12484725-12484923 | Rare:49 |