| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:74148331-74148599 | Common:2; Rare:86 | ||||
| chr18:74291871-74292112 | Common:1; Rare:73 | ||||
| chr18:74496065-74496416 | Common:4; Rare:113 | ||||
| chr18:74597801-74597898 | Common:1; Rare:25 | ||||
| chr18:79988264-79988655 | Common:3; Rare:126; Clinvar:1; Clinvar (pathogenic):2 | ||||
| chr19:344784-344951 | Common:3; Rare:61 | ||||
| chr19:507463-507506 | Rare:13 | ||||
| chr19:572237-572610 | Common:3; Rare:179 | ||||
| chr19:633520-633745 | Common:8; Rare:99 | ||||
| chr19:663147-663436 | Common:2; Rare:119 | ||||
| chr19:893165-893484 | Common:3; Rare:133 | ||||
| chr19:984225-984406 | Common:1; Rare:73 | ||||
| chr19:1103801-1104115 | Common:4; Rare:131 | ||||
| chr19:1132153-1132328 | Rare:78 | ||||
| chr19:1354705-1354996 | Common:3; Rare:120 |