| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:37655413-37655588 | Common:3; Rare:73 | ||||
| chr19:37692172-37692392 | Common:2; Rare:43 | ||||
| chr19:37779546-37779662 | Rare:26 | ||||
| chr19:37817279-37817601 | Common:1; Rare:67 | ||||
| chr19:37907039-37907340 | Rare:64 | ||||
| chr19:38264270-38264995 | Common:7; Rare:194 | ||||
| chr19:38315755-38316104 | Rare:120 | ||||
| chr19:38374393-38374860 | Rare:185 | ||||
| chr19:38388385-38388717 | Common:1; Rare:82 | ||||
| chr19:38618767-38619323 | Common:4; Rare:153 | ||||
| chr19:38647372-38647858 | Common:3; Rare:159 | ||||
| chr19:38724226-38724562 | Common:2; Rare:113; Clinvar:1; Clinvar (benign):3 | ||||
| chr19:38736969-38737119 | Common:2; Rare:18 | ||||
| chr19:38831086-38831398 | Common:2; Rare:122 | ||||
| chr19:38831721-38832045 | Common:4; Rare:110; Clinvar (benign):1 |