| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:1105175-1105804 | Common:4; Rare:281; Clinvar (pathogenic):1 | ||||
| chr19:1132109-1132490 | Common:2; Rare:153 | ||||
| chr19:1155088-1155340 | Rare:76 | ||||
| chr19:1168736-1168862 | Common:1; Rare:32 | ||||
| chr19:1169165-1169316 | Common:1; Rare:41 | ||||
| chr19:1174225-1174425 | Common:2; Rare:86 | ||||
| chr19:1248423-1248588 | Common:1; Rare:51 | ||||
| chr19:1251426-1251598 | Rare:82 | ||||
| chr19:1260891-1261179 | Common:3; Rare:97 | ||||
| chr19:1269036-1269370 | Common:3; Rare:127 | ||||
| chr19:1354779-1355008 | Common:2; Rare:97 | ||||
| chr19:1383419-1383492 | Rare:38 | ||||
| chr19:1942586-1942609 | Rare:7 | ||||
| chr19:2085307-2085528 | Common:4; Rare:55 | ||||
| chr19:2096232-2096415 | Rare:61 |