| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:39403695-39404049 | Rare:67 | ||||
| chr19:39409633-39409877 | Common:1; Rare:60 | ||||
| chr19:39411454-39411710 | Common:2; Rare:48 | ||||
| chr19:40744785-40745058 | Common:4; Rare:61 | ||||
| chr19:40810794-40811130 | Common:4; Rare:79 | ||||
| chr19:40923975-40924492 | Common:1; Rare:144 | ||||
| chr19:40928799-40928899 | Rare:28 | ||||
| chr19:40936034-40936551 | Rare:177 | ||||
| chr19:40941058-40941488 | Common:5; Rare:108 | ||||
| chr19:40941743-40942224 | Common:10; Rare:155 | ||||
| chr19:40949043-40949249 | Common:2; Rare:41 | ||||
| chr19:41352770-41352857 | Rare:26 | ||||
| chr19:41352898-41353157 | Common:4; Rare:76; Clinvar (benign):2 | ||||
| chr19:41424305-41424453 | Common:1; Rare:42; Clinvar:1 | ||||
| chr19:41500608-41500782 | Common:1; Rare:31 |