| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:1103755-1104124 | Common:7; Rare:155 | ||||
| chr19:1131886-1132239 | Common:3; Rare:135 | ||||
| chr19:1241534-1241820 | Rare:82 | ||||
| chr19:1251388-1251656 | Common:2; Rare:109 | ||||
| chr19:1251743-1251813 | Common:1; Rare:27 | ||||
| chr19:1269028-1269381 | Common:3; Rare:131 | ||||
| chr19:1275788-1276159 | Common:2; Rare:157 | ||||
| chr19:1354720-1355029 | Common:3; Rare:142 | ||||
| chr19:1401471-1401836 | Common:2; Rare:97; Clinvar:1; Clinvar (benign):4 | ||||
| chr19:1407639-1407957 | Common:1; Rare:88 | ||||
| chr19:1479554-1479635 | Rare:18 | ||||
| chr19:1512976-1513329 | Common:1; Rare:122 | ||||
| chr19:1605361-1605512 | Common:1; Rare:65 | ||||
| chr19:1622136-1622359 | Rare:88 | ||||
| chr19:1812198-1812505 | Common:3; Rare:90 |