| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:35972462-35972744 | Common:3; Rare:99 | ||||
| chr18:36067257-36067628 | Common:2; Rare:123 | ||||
| chr18:36129189-36129484 | Common:4; Rare:86 | ||||
| chr18:36129772-36129951 | Common:1; Rare:74 | ||||
| chr18:36187362-36187587 | Common:4; Rare:78 | ||||
| chr18:36692873-36693149 | Common:2; Rare:40 | ||||
| chr18:36828682-36829294 | Common:3; Rare:232 | ||||
| chr18:44680696-44680995 | Common:1; Rare:84; Clinvar:2; Clinvar (benign):1 | ||||
| chr18:45967243-45967510 | Rare:103 | ||||
| chr18:46098189-46098558 | Common:11; Rare:116; Clinvar (benign):7 | ||||
| chr18:46104135-46104414 | Common:4; Rare:82; Clinvar (benign):1 | ||||
| chr18:46756795-46756944 | Common:2; Rare:47 | ||||
| chr18:46917351-46917659 | Common:3; Rare:136 | ||||
| chr18:47150395-47150570 | Common:4; Rare:69 | ||||
| chr18:47930204-47930308 | Rare:41 |