| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:38724153-38724564 | Common:2; Rare:137; Clinvar:1; Clinvar (benign):3 | ||||
| chr19:38735610-38735992 | Common:4; Rare:23 | ||||
| chr19:38831667-38831731 | Common:2; Rare:18 | ||||
| chr19:38831745-38832071 | Common:4; Rare:105; Clinvar (benign):1 | ||||
| chr19:38842208-38842650 | Rare:83 | ||||
| chr19:38842699-38842850 | Rare:31 | ||||
| chr19:38852319-38852482 | Rare:41 | ||||
| chr19:38899514-38900216 | Rare:193 | ||||
| chr19:38916031-38916238 | Common:1; Rare:80; Clinvar:2; Clinvar (benign):2 | ||||
| chr19:38930708-38931053 | Common:3; Rare:103; Clinvar:2; Clinvar (benign):3 | ||||
| chr19:38952903-38953010 | Common:2; Rare:22 | ||||
| chr19:39342406-39342574 | Common:3; Rare:58 | ||||
| chr19:39384957-39385269 | Rare:52 | ||||
| chr19:39386432-39386799 | Rare:97 | ||||
| chr19:39388972-39389129 | Common:1; Rare:43 |