| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:63422377-63422577 | Rare:56 | ||||
| chr18:68714977-68715263 | Common:6; Rare:126 | ||||
| chr18:70205659-70205760 | Common:2; Rare:46; Clinvar (benign):2 | ||||
| chr18:74148358-74148629 | Common:1; Rare:73 | ||||
| chr18:74291897-74292255 | Common:3; Rare:103 | ||||
| chr18:74496021-74496434 | Common:4; Rare:132 | ||||
| chr18:74499776-74500028 | Common:2; Rare:66 | ||||
| chr18:74597584-74597914 | Common:2; Rare:88 | ||||
| chr18:76822275-76822615 | Common:11; Rare:92 | ||||
| chr18:79679279-79679413 | Rare:76 | ||||
| chr18:79988356-79988717 | Common:5; Rare:134; Clinvar:1; Clinvar (pathogenic):2 | ||||
| chr19:344784-344914 | Common:3; Rare:40 | ||||
| chr19:572237-572649 | Common:3; Rare:209 | ||||
| chr19:633497-633724 | Common:8; Rare:113 | ||||
| chr19:804912-805085 | Common:1; Rare:86 |