| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:45406340-45406649 | Common:1; Rare:67 | ||||
| chr19:45507228-45507508 | Common:1; Rare:72 | ||||
| chr19:45584761-45585074 | Common:4; Rare:117; Clinvar:2; Clinvar (benign):4 | ||||
| chr19:45730857-45731092 | Common:1; Rare:54 | ||||
| chr19:45769153-45769314 | Rare:43 | ||||
| chr19:45769323-45769470 | Common:1; Rare:75 | ||||
| chr19:46296836-46297069 | Common:4; Rare:88 | ||||
| chr19:46346938-46347124 | Common:3; Rare:56 | ||||
| chr19:46413434-46413762 | Common:1; Rare:94 | ||||
| chr19:46471484-46471619 | Common:5; Rare:54 | ||||
| chr19:46495859-46495975 | Rare:37 | ||||
| chr19:46600913-46601420 | Common:5; Rare:175; Clinvar (benign):1 | ||||
| chr19:47112158-47112339 | Rare:54 | ||||
| chr19:47130653-47131005 | Common:1; Rare:113 | ||||
| chr19:47256472-47256583 | Rare:42 |