| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:52189585-52190100 | Common:7; Rare:285 | ||||
| chr19:52269427-52269606 | Common:2; Rare:123 | ||||
| chr19:52397755-52397876 | Common:2; Rare:33 | ||||
| chr19:52397781-52397897 | Common:4; Rare:39 | ||||
| chr19:52786712-52786932 | Common:17; Rare:96 | ||||
| chr19:53467571-53467769 | Common:3; Rare:52 | ||||
| chr19:53520660-53521200 | Common:34; Rare:215 | ||||
| chr19:53537824-53538200 | Common:13; Rare:262 | ||||
| chr19:53865293-53865723 | Common:2; Rare:80 | ||||
| chr19:53865783-53866420 | Common:5; Rare:198 | ||||
| chr19:53867678-53867940 | Common:2; Rare:136 | ||||
| chr19:53869150-53869900 | Common:9; Rare:306 | ||||
| chr19:53879370-53879780 | Common:8; Rare:168 | ||||
| chr19:54102669-54102894 | Common:6; Rare:113 | ||||
| chr19:54115260-54115500 | Common:3; Rare:96; Clinvar (benign):3 |