| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:31042930-31042977 | Rare:9 | ||||
| chr18:31101250-31101622 | Common:11; Rare:102 | ||||
| chr18:31101901-31101999 | Common:1; Rare:26; Clinvar:4; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr18:31102014-31102307 | Common:1; Rare:53; Clinvar:5 | ||||
| chr18:31102398-31102516 | Rare:34 | ||||
| chr18:31498081-31498279 | Common:1; Rare:70; Clinvar:5; Clinvar (benign):6 | ||||
| chr18:31943098-31943380 | Common:7; Rare:92 | ||||
| chr18:32018513-32018832 | Common:2; Rare:101 | ||||
| chr18:32091740-32091969 | Common:5; Rare:75 | ||||
| chr18:32092384-32092767 | Common:5; Rare:173 | ||||
| chr18:33578256-33578555 | Common:4; Rare:83 | ||||
| chr18:34593188-34593390 | Rare:42 | ||||
| chr18:34976942-34977061 | Common:1; Rare:20 | ||||
| chr18:35041244-35041460 | Common:1; Rare:80 | ||||
| chr18:35240888-35241094 | Common:2; Rare:79 |