| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:18594391-18594493 | Rare:30 | ||||
| chr19:18636738-18637047 | Common:2; Rare:77 | ||||
| chr19:18683495-18683694 | Common:1; Rare:65 | ||||
| chr19:18919344-18919740 | Common:2; Rare:139 | ||||
| chr19:18941233-18941454 | Common:4; Rare:58 | ||||
| chr19:19033437-19033653 | Common:2; Rare:74 | ||||
| chr19:19033820-19033930 | Common:1; Rare:31 | ||||
| chr19:19033978-19034128 | Common:1; Rare:30 | ||||
| chr19:19105709-19105823 | Common:1; Rare:39; Clinvar (pathogenic):1 | ||||
| chr19:19192098-19192212 | Common:1; Rare:40 | ||||
| chr19:19192624-19192976 | Common:2; Rare:83 | ||||
| chr19:19211818-19212040 | Rare:56 | ||||
| chr19:19320476-19320850 | Common:4; Rare:136 | ||||
| chr19:19516161-19516253 | Rare:46 | ||||
| chr19:19628496-19628681 | Rare:33 |