| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:74148358-74148552 | Common:1; Rare:60 | ||||
| chr18:74291906-74292267 | Common:4; Rare:108 | ||||
| chr18:74496066-74496407 | Common:4; Rare:109 | ||||
| chr18:74499806-74499953 | Common:2; Rare:33 | ||||
| chr18:74597570-74597929 | Common:2; Rare:98 | ||||
| chr18:79679279-79679584 | Common:1; Rare:151 | ||||
| chr18:79988356-79988661 | Common:4; Rare:110; Clinvar:1; Clinvar (pathogenic):2 | ||||
| chr19:344778-344945 | Common:3; Rare:58 | ||||
| chr19:572322-572649 | Rare:174 | ||||
| chr19:633520-633736 | Common:8; Rare:99 | ||||
| chr19:663143-663430 | Common:2; Rare:114 | ||||
| chr19:893167-893484 | Common:3; Rare:132 | ||||
| chr19:984240-984401 | Rare:63 | ||||
| chr19:1021256-1021522 | Common:10; Rare:114 | ||||
| chr19:1103787-1104119 | Common:4; Rare:141 |