| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:12308465-12308796 | Common:6; Rare:105 | ||||
| chr18:12376971-12377011 | Rare:14; Clinvar (benign):1 | ||||
| chr18:12657981-12658230 | Common:6; Rare:96 | ||||
| chr18:12702612-12703147 | Common:3; Rare:210 | ||||
| chr18:12947638-12948094 | Common:3; Rare:131 | ||||
| chr18:12991131-12991410 | Common:2; Rare:104 | ||||
| chr18:13726509-13726765 | Common:3; Rare:92 | ||||
| chr18:21111548-21111923 | Common:2; Rare:117 | ||||
| chr18:21600626-21600984 | Common:2; Rare:93 | ||||
| chr18:22169385-22169622 | Common:1; Rare:60 | ||||
| chr18:22170349-22170499 | Rare:36 | ||||
| chr18:22933204-22933561 | Common:5; Rare:114; Clinvar:7; Clinvar (benign):3 | ||||
| chr18:22933781-22933912 | Common:1; Rare:54 | ||||
| chr18:23453153-23453333 | Rare:62 | ||||
| chr18:23453422-23453484 | Rare:15 |