| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:7535402-7535740 | Common:3; Rare:100; Clinvar:2 | ||||
| chr19:7629531-7629854 | Common:5; Rare:115; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr19:7943625-7943988 | Rare:102 | ||||
| chr19:8005532-8005821 | Common:1; Rare:101 | ||||
| chr19:8308328-8308638 | Common:2; Rare:89 | ||||
| chr19:8321324-8321568 | Common:2; Rare:113 | ||||
| chr19:8390077-8390402 | Common:1; Rare:94 | ||||
| chr19:9435512-9435602 | Rare:36 | ||||
| chr19:9621192-9621548 | Common:3; Rare:99 | ||||
| chr19:9818809-9818856 | Rare:17 | ||||
| chr19:9827823-9827982 | Common:1; Rare:58 | ||||
| chr19:10333517-10333699 | Rare:62 | ||||
| chr19:10380503-10380825 | Common:12; Rare:90; Clinvar:5 | ||||
| chr19:10403475-10403678 | Rare:104 | ||||
| chr19:10577225-10577567 | Common:2; Rare:81 |