| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:5544230-5544344 | Common:1; Rare:18 | ||||
| chr18:7117704-7117914 | Common:3; Rare:71 | ||||
| chr18:7946844-7946946 | Rare:24 | ||||
| chr18:8707634-8707861 | Rare:42 | ||||
| chr18:9102475-9102772 | Common:2; Rare:124; Clinvar:6; Clinvar (benign):2 | ||||
| chr18:9136492-9136855 | Rare:138 | ||||
| chr18:9136975-9137059 | Common:1; Rare:29 | ||||
| chr18:9475357-9475685 | Common:4; Rare:90 | ||||
| chr18:9913719-9914133 | Common:1; Rare:143 | ||||
| chr18:9914185-9914301 | Rare:53 | ||||
| chr18:10525843-10526108 | Common:2; Rare:102 | ||||
| chr18:11851242-11851498 | Common:3; Rare:96 | ||||
| chr18:11857581-11857768 | Common:1; Rare:43 | ||||
| chr18:11908267-11908442 | Rare:51 | ||||
| chr18:11980859-11981025 | Common:3; Rare:55 |