| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:42268150-42268620 | Rare:94 | ||||
| chr19:42268641-42269255 | Rare:249 | ||||
| chr19:42280392-42280606 | Rare:54 | ||||
| chr19:42283739-42284125 | Rare:128 | ||||
| chr19:42301804-42302204 | Rare:138 | ||||
| chr19:42302325-42302707 | Rare:108 | ||||
| chr19:42325349-42325692 | Rare:102 | ||||
| chr19:42352568-42352968 | Common:2; Rare:149; Clinvar (benign):2 | ||||
| chr19:42423186-42423360 | Common:1; Rare:40 | ||||
| chr19:42423567-42423759 | Common:2; Rare:64 | ||||
| chr19:43463650-43464060 | Rare:120 | ||||
| chr19:43504040-43504440 | Common:7; Rare:118 | ||||
| chr19:43504610-43505010 | Common:2; Rare:134 | ||||
| chr19:43527169-43527392 | Common:5; Rare:79; Clinvar:3; Clinvar (benign):7; Clinvar (pathogenic):2 | ||||
| chr19:43533102-43533400 | Common:2; Rare:90 |