| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:46173329-46173604 | Common:1; Rare:58 | ||||
| chr18:46173898-46174140 | Common:1; Rare:57 | ||||
| chr18:46333576-46333701 | Rare:37 | ||||
| chr18:46333767-46334103 | Common:2; Rare:82 | ||||
| chr18:46917410-46917614 | Rare:81 | ||||
| chr18:46946550-46946860 | Common:3; Rare:72 | ||||
| chr18:47150083-47150225 | Common:1; Rare:41 | ||||
| chr18:47150371-47150657 | Common:4; Rare:111 | ||||
| chr18:47176275-47176469 | Common:1; Rare:83; Clinvar (benign):1 | ||||
| chr18:47930690-47931040 | Rare:113 | ||||
| chr18:47931055-47931359 | Common:1; Rare:116 | ||||
| chr18:47931445-47931845 | Common:3; Rare:140 | ||||
| chr18:48410280-48410580 | Common:5; Rare:77 | ||||
| chr18:48538889-48539192 | Common:1; Rare:73 | ||||
| chr18:48539452-48540677 | Common:4; Rare:323 |