| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:21111568-21112150 | Common:8; Rare:425 | ||||
| chr18:21242140-21242429 | Common:3; Rare:243 | ||||
| chr18:21242585-21243690 | Common:7; Rare:304 | ||||
| chr18:21599900-21601151 | Common:7; Rare:652 | ||||
| chr18:21612171-21612444 | Common:3; Rare:217 | ||||
| chr18:21612460-21612900 | Common:3; Rare:191 | ||||
| chr18:21703475-21704340 | Common:1; Rare:428 | ||||
| chr18:21704564-21705039 | Common:8; Rare:329 | ||||
| chr18:21740612-21741081 | Common:5; Rare:211 | ||||
| chr18:21741159-21741560 | Common:4; Rare:175; Clinvar (benign):2 | ||||
| chr18:22169311-22169683 | Common:3; Rare:215 | ||||
| chr18:22169836-22170141 | Common:3; Rare:86 | ||||
| chr18:22170298-22170449 | Rare:43 | ||||
| chr18:22933167-22933532 | Common:10; Rare:267; Clinvar:14; Clinvar (benign):7 | ||||
| chr18:22933648-22933967 | Common:5; Rare:286 |