| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:2926765-2927069 | Common:2; Rare:69; Clinvar:3 | ||||
| chr18:2946587-2946825 | Common:1; Rare:44 | ||||
| chr18:2951268-2951588 | Common:1; Rare:71; Clinvar:1; Clinvar (benign):1 | ||||
| chr18:3593812-3594127 | Common:3; Rare:51 | ||||
| chr18:3594277-3594492 | Rare:44 | ||||
| chr18:3603593-3603740 | Rare:18 | ||||
| chr18:5238006-5238139 | Common:1; Rare:51 | ||||
| chr18:6462536-6462698 | Common:4; Rare:35 | ||||
| chr18:9565403-9565699 | Rare:42 | ||||
| chr18:9828319-9828333 | Rare:2 | ||||
| chr18:9828336-9828448 | Common:2; Rare:24 | ||||
| chr18:9838870-9838971 | Common:1; Rare:23 | ||||
| chr18:11947735-11947919 | Common:1; Rare:24 | ||||
| chr18:12370854-12371167 | Common:1; Rare:75; Clinvar (benign):2 | ||||
| chr18:12885655-12885824 | Common:2; Rare:31 |