| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:11952170-11952410 | Rare:30 | ||||
| chr18:12366930-12367651 | Common:4; Rare:249; Clinvar:8; Clinvar (benign):13 | ||||
| chr18:12838000-12838450 | Rare:145 | ||||
| chr18:12883108-12883388 | Common:1; Rare:88 | ||||
| chr18:21315854-21316298 | Common:5; Rare:143 | ||||
| chr18:22226840-22227150 | Common:6; Rare:97 | ||||
| chr18:22282500-22282860 | Common:4; Rare:90 | ||||
| chr18:23982480-23982850 | Common:1; Rare:133 | ||||
| chr18:24015501-24015732 | Common:3; Rare:41 | ||||
| chr18:26548512-26548752 | Common:2; Rare:76 | ||||
| chr18:26746600-26746810 | Rare:34 | ||||
| chr18:36186480-36186957 | Common:2; Rare:183 | ||||
| chr18:37393988-37394460 | Common:7; Rare:300 | ||||
| chr18:37403010-37403400 | Rare:120 | ||||
| chr18:37409810-37410240 | Rare:161 |