| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:63970002-63970133 | Rare:25 | ||||
| chr18:66604090-66604377 | Common:4; Rare:53 | ||||
| chr18:68714987-68715317 | Common:7; Rare:137 | ||||
| chr18:70205648-70205763 | Common:2; Rare:51; Clinvar (benign):2 | ||||
| chr18:70288678-70289072 | Common:6; Rare:127 | ||||
| chr18:74148342-74148546 | Common:2; Rare:67 | ||||
| chr18:74291855-74292272 | Common:4; Rare:124; Clinvar:1 | ||||
| chr18:74496015-74496434 | Common:4; Rare:136 | ||||
| chr18:74500773-74501007 | Common:1; Rare:51 | ||||
| chr18:74597385-74597475 | Common:1; Rare:26 | ||||
| chr18:74597584-74597914 | Common:2; Rare:88 | ||||
| chr18:79679240-79679584 | Common:2; Rare:168 | ||||
| chr18:79988356-79988661 | Common:4; Rare:110; Clinvar:1; Clinvar (pathogenic):2 | ||||
| chr19:344786-344928 | Common:3; Rare:46 | ||||
| chr19:572300-572661 | Common:1; Rare:185 |