| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:35344401-35344534 | Common:2; Rare:43 | ||||
| chr18:36129263-36129471 | Common:3; Rare:63 | ||||
| chr18:36187388-36187516 | Common:1; Rare:47 | ||||
| chr18:36828736-36829138 | Common:3; Rare:153 | ||||
| chr18:45967265-45967503 | Rare:84 | ||||
| chr18:46104135-46104412 | Common:4; Rare:80; Clinvar (benign):1 | ||||
| chr18:46173991-46174081 | Common:1; Rare:28 | ||||
| chr18:47150452-47150546 | Common:2; Rare:34 | ||||
| chr18:49813506-49813589 | Rare:18 | ||||
| chr18:49813826-49814062 | Common:1; Rare:103 | ||||
| chr18:50967884-50968058 | Rare:61 | ||||
| chr18:62186987-62187305 | Common:5; Rare:91 | ||||
| chr18:63422375-63422648 | Common:1; Rare:70 | ||||
| chr18:68715002-68715205 | Common:2; Rare:90 | ||||
| chr18:70205659-70205763 | Common:2; Rare:46; Clinvar (benign):2 |