| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:7488995-7489103 | Rare:48 | ||||
| chr19:7534113-7534202 | Common:3; Rare:22; Clinvar (benign):1 | ||||
| chr19:7535543-7535787 | Common:3; Rare:89; Clinvar:2 | ||||
| chr19:7629535-7629848 | Common:5; Rare:111; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr19:7874290-7874525 | Common:1; Rare:56 | ||||
| chr19:7943641-7943990 | Rare:92 | ||||
| chr19:8005520-8005821 | Common:1; Rare:105 | ||||
| chr19:8308312-8308638 | Common:2; Rare:99 | ||||
| chr19:8321308-8321703 | Common:2; Rare:159 | ||||
| chr19:8390036-8390449 | Common:2; Rare:115 | ||||
| chr19:8444818-8445046 | Common:2; Rare:107 | ||||
| chr19:8514144-8514194 | Rare:15 | ||||
| chr19:9140311-9140428 | Rare:31 | ||||
| chr19:9435559-9435641 | Common:1; Rare:30 | ||||
| chr19:9538596-9538736 | Common:1; Rare:46 |