| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:31101250-31101633 | Common:11; Rare:104 | ||||
| chr18:31101901-31102102 | Common:1; Rare:51; Clinvar:5; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr18:31102354-31102506 | Rare:44; Clinvar:2 | ||||
| chr18:31498082-31498344 | Common:1; Rare:95; Clinvar:8; Clinvar (benign):7 | ||||
| chr18:31943098-31943380 | Common:7; Rare:92 | ||||
| chr18:32018648-32018860 | Common:2; Rare:63 | ||||
| chr18:32091842-32091907 | Common:1; Rare:24 | ||||
| chr18:32092384-32092727 | Common:5; Rare:156 | ||||
| chr18:33578187-33578528 | Common:4; Rare:93 | ||||
| chr18:34593167-34593408 | Rare:46 | ||||
| chr18:34976942-34977067 | Common:1; Rare:22 | ||||
| chr18:35240917-35241094 | Common:2; Rare:66 | ||||
| chr18:35290150-35290391 | Common:2; Rare:78 | ||||
| chr18:35344394-35344505 | Common:2; Rare:38 | ||||
| chr18:35972454-35972770 | Common:4; Rare:112 |