| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:70205970-70206164 | Rare:63 | ||||
| chr18:74148353-74148619 | Common:1; Rare:76 | ||||
| chr18:74291862-74292267 | Common:4; Rare:121 | ||||
| chr18:74496021-74496427 | Common:4; Rare:132 | ||||
| chr18:74499773-74499946 | Common:2; Rare:35 | ||||
| chr18:74597385-74597439 | Common:1; Rare:10 | ||||
| chr18:74597573-74597914 | Common:2; Rare:90 | ||||
| chr18:75210667-75210901 | Common:3; Rare:49; Clinvar:7 | ||||
| chr18:76822236-76822646 | Common:11; Rare:116 | ||||
| chr18:79679261-79679603 | Common:1; Rare:168 | ||||
| chr18:79964584-79964722 | Common:1; Rare:42 | ||||
| chr18:79988240-79988671 | Common:4; Rare:137; Clinvar:1; Clinvar (pathogenic):2 | ||||
| chr19:344778-344957 | Common:3; Rare:65 | ||||
| chr19:572216-572649 | Common:4; Rare:213 | ||||
| chr19:582326-582529 | Common:3; Rare:70 |