| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:44679627-44680193 | Common:2; Rare:188 | ||||
| chr18:44680159-44681040 | Common:4; Rare:454; Clinvar:6; Clinvar (benign):3 | ||||
| chr18:45967179-45967604 | Common:1; Rare:360; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
| chr18:46072197-46072395 | Common:3; Rare:79 | ||||
| chr18:46091745-46092174 | Common:5; Rare:135; Clinvar (benign):3 | ||||
| chr18:46098195-46098618 | Common:26; Rare:294; Clinvar (benign):19 | ||||
| chr18:46104176-46104495 | Common:9; Rare:216 | ||||
| chr18:46104533-46105477 | Common:11; Rare:322 | ||||
| chr18:46173404-46173643 | Rare:110 | ||||
| chr18:46173836-46174189 | Common:5; Rare:206 | ||||
| chr18:46333832-46334068 | Common:2; Rare:103 | ||||
| chr18:46917316-46917710 | Common:7; Rare:388 | ||||
| chr18:46917690-46918509 | Common:9; Rare:350 | ||||
| chr18:46946510-46947210 | Common:11; Rare:285 | ||||
| chr18:46947130-46947520 | Common:6; Rare:85 |