| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:3366535-3366634 | Common:3; Rare:35 | ||||
| chr19:4182541-4182713 | Common:1; Rare:62 | ||||
| chr19:4518455-4518656 | Common:4; Rare:54 | ||||
| chr19:4639231-4639573 | Common:1; Rare:113 | ||||
| chr19:4723753-4723853 | Common:1; Rare:32 | ||||
| chr19:4867621-4867884 | Common:4; Rare:78 | ||||
| chr19:5293179-5293425 | Common:1; Rare:105 | ||||
| chr19:5622583-5623355 | Common:6; Rare:304 | ||||
| chr19:5680492-5680772 | Rare:82 | ||||
| chr19:5978078-5978393 | Common:3; Rare:117 | ||||
| chr19:6710807-6711065 | Common:2; Rare:82; Clinvar:1; Clinvar (benign):1 | ||||
| chr19:6714177-6714433 | Common:1; Rare:74; Clinvar (benign):2 | ||||
| chr19:6740819-6741051 | Rare:65 | ||||
| chr19:7395014-7395199 | Common:6; Rare:57 | ||||
| chr19:7535574-7535739 | Common:3; Rare:55 |