| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:12613386-12613717 | Common:3; Rare:64 | ||||
| chr19:12613793-12614127 | Common:3; Rare:51 | ||||
| chr19:12665265-12665436 | Rare:45; Clinvar:1; Clinvar (pathogenic):2 | ||||
| chr19:12782364-12782447 | Rare:18 | ||||
| chr19:12782453-12782772 | Common:5; Rare:111 | ||||
| chr19:12786223-12786425 | Common:1; Rare:42 | ||||
| chr19:12788934-12789316 | Common:5; Rare:80 | ||||
| chr19:12789790-12790146 | Common:1; Rare:78 | ||||
| chr19:12793482-12793595 | Common:2; Rare:32 | ||||
| chr19:12793851-12794053 | Rare:38 | ||||
| chr19:12867603-12867834 | Common:1; Rare:87 | ||||
| chr19:12885108-12885486 | Rare:109; Clinvar (pathogenic):2 | ||||
| chr19:12937462-12937556 | Common:1; Rare:16 | ||||
| chr19:12937937-12938047 | Common:1; Rare:25 | ||||
| chr19:13012838-13013107 | Common:5; Rare:54 |