| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:1026496-1026717 | Rare:81 | ||||
| chr19:1039888-1040212 | Common:2; Rare:107 | ||||
| chr19:1042306-1042459 | Rare:71 | ||||
| chr19:1066998-1067187 | Common:1; Rare:54 | ||||
| chr19:1071596-1071669 | Common:1; Rare:15 | ||||
| chr19:1095284-1095613 | Common:8; Rare:145 | ||||
| chr19:1103710-1104139 | Common:8; Rare:172 | ||||
| chr19:1104326-1104795 | Common:5; Rare:108 | ||||
| chr19:1131821-1131906 | Rare:29 | ||||
| chr19:1132188-1132407 | Rare:86 | ||||
| chr19:1174185-1174388 | Common:1; Rare:95 | ||||
| chr19:1205485-1205866 | Common:2; Rare:123; Clinvar:1 | ||||
| chr19:1207128-1207213 | Common:1; Rare:22; Clinvar:3; Clinvar (benign):12; Clinvar (pathogenic):1 | ||||
| chr19:1237830-1238171 | Common:2; Rare:104 | ||||
| chr19:1241595-1241839 | Rare:79 |