| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:185395896-185396082 | Rare:58 | ||||
| chr4:185396396-185396704 | Rare:106 | ||||
| chr4:185425861-185426256 | Common:4; Rare:122 | ||||
| chr4:185471070-185471550 | Common:11; Rare:97 | ||||
| chr4:185535459-185535624 | Common:1; Rare:53; Clinvar (benign):2 | ||||
| chr4:185810953-185811123 | Common:1; Rare:40 | ||||
| chr4:185812127-185812296 | Rare:33 | ||||
| chr4:186144580-186144920 | Common:3; Rare:101 | ||||
| chr4:186191359-186191679 | Common:4; Rare:93; Clinvar:2; Clinvar (benign):3 | ||||
| chr4:186266148-186266926 | Common:5; Rare:173; Clinvar (benign):2 | ||||
| chr4:186554461-186555324 | Common:3; Rare:300 | ||||
| chr4:186722985-186723801 | Common:17; Rare:325 | ||||
| chr4:186723804-186724036 | Common:6; Rare:77 | ||||
| chr4:186724050-186724362 | Common:2; Rare:72 | ||||
| chr4:186726644-186726834 | Common:4; Rare:62 |