| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:7567757-7567831 | Common:1; Rare:22 | ||||
| chr18:8704542-8704674 | Common:1; Rare:27 | ||||
| chr18:9129630-9129825 | Common:1; Rare:21 | ||||
| chr18:9138624-9138820 | Common:3; Rare:34 | ||||
| chr18:10041128-10041390 | Common:3; Rare:45 | ||||
| chr18:11149530-11149710 | Rare:62 | ||||
| chr18:11851945-11852406 | Common:4; Rare:143 | ||||
| chr18:11947752-11947799 | Common:1; Rare:7 | ||||
| chr18:12329673-12329930 | Common:1; Rare:58; Clinvar:1 | ||||
| chr18:12337441-12337629 | Rare:54; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):2 | ||||
| chr18:12344238-12344515 | Common:3; Rare:87; Clinvar (benign):1 | ||||
| chr18:12346412-12346564 | Common:1; Rare:32 | ||||
| chr18:21831399-21831617 | Rare:37 | ||||
| chr18:22001847-22002119 | Common:3; Rare:65 | ||||
| chr18:22084643-22084827 | Rare:38 |