| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:23586416-23586528 | Common:2; Rare:54; Clinvar:3; Clinvar (benign):1 | ||||
| chr18:23872687-23873047 | Rare:89; Clinvar (pathogenic):1 | ||||
| chr18:24426486-24426757 | Common:5; Rare:110 | ||||
| chr18:31497985-31498247 | Common:1; Rare:77; Clinvar:4; Clinvar (benign):3 | ||||
| chr18:35290223-35290377 | Common:1; Rare:54 | ||||
| chr18:35972472-35972693 | Common:3; Rare:66 | ||||
| chr18:36129826-36129924 | Rare:39 | ||||
| chr18:36828971-36829132 | Common:3; Rare:58 | ||||
| chr18:46098236-46098588 | Common:11; Rare:97; Clinvar (benign):6 | ||||
| chr18:46104136-46104406 | Common:4; Rare:79; Clinvar (benign):1 | ||||
| chr18:47150463-47150567 | Common:3; Rare:37 | ||||
| chr18:49487192-49487472 | Common:3; Rare:116 | ||||
| chr18:50374904-50375083 | Common:1; Rare:59 | ||||
| chr18:57586595-57586845 | Rare:67 | ||||
| chr18:59359240-59359515 | Common:3; Rare:116; Clinvar:1 |