| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:17405289-17406093 | Common:11; Rare:195; Clinvar:1 | ||||
| chr19:17468592-17468780 | Common:1; Rare:32 | ||||
| chr19:17511448-17511820 | Common:4; Rare:155 | ||||
| chr19:17751369-17751517 | Common:1; Rare:38 | ||||
| chr19:18086898-18087011 | Common:2; Rare:38; Clinvar (benign):1 | ||||
| chr19:18152933-18153287 | Common:1; Rare:115 | ||||
| chr19:18173539-18173886 | Common:1; Rare:69 | ||||
| chr19:18203972-18204356 | Common:2; Rare:119 | ||||
| chr19:18280096-18280599 | Common:4; Rare:183 | ||||
| chr19:18323018-18323232 | Common:3; Rare:75 | ||||
| chr19:18433171-18433308 | Rare:49 | ||||
| chr19:18433406-18433880 | Common:11; Rare:170 | ||||
| chr19:18438102-18438274 | Rare:57 | ||||
| chr19:18539383-18539663 | Common:4; Rare:93 | ||||
| chr19:18557656-18557911 | Common:5; Rare:68 |