| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:21612187-21612444 | Common:2; Rare:139 | ||||
| chr18:21703815-21704191 | Rare:112 | ||||
| chr18:21704537-21705001 | Common:8; Rare:281 | ||||
| chr18:21740593-21740906 | Common:6; Rare:186 | ||||
| chr18:21740900-21741420 | Common:5; Rare:214 | ||||
| chr18:22169311-22169654 | Common:4; Rare:169 | ||||
| chr18:22933235-22933454 | Common:5; Rare:154; Clinvar:8; Clinvar (benign):4 | ||||
| chr18:22933751-22933933 | Common:2; Rare:143 | ||||
| chr18:23135339-23135487 | Common:1; Rare:33 | ||||
| chr18:23437817-23438047 | Common:4; Rare:92 | ||||
| chr18:23453063-23453349 | Rare:168 | ||||
| chr18:23503275-23503579 | Common:4; Rare:209 | ||||
| chr18:23586396-23586573 | Common:4; Rare:146; Clinvar:6; Clinvar (benign):2 | ||||
| chr18:23586669-23587059 | Common:3; Rare:150 | ||||
| chr18:23662753-23663006 | Common:8; Rare:152 |