| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:6640490-6640690 | Common:2; Rare:85 | ||||
| chr4:10457367-10457481 | Common:2; Rare:44 | ||||
| chr4:13627723-13627859 | Common:1; Rare:41 | ||||
| chr4:15681477-15681875 | Common:4; Rare:138 | ||||
| chr4:17614553-17614647 | Common:2; Rare:40 | ||||
| chr4:17810629-17811035 | Common:3; Rare:125 | ||||
| chr4:25914029-25914291 | Common:2; Rare:114 | ||||
| chr4:26320440-26320792 | Common:1; Rare:102 | ||||
| chr4:26583982-26584094 | Rare:22 | ||||
| chr4:37826534-37826729 | Common:6; Rare:70 | ||||
| chr4:38867612-38867816 | Common:2; Rare:75 | ||||
| chr4:39458857-39459112 | Common:3; Rare:147; Clinvar (benign):5 | ||||
| chr4:39638853-39639140 | Common:1; Rare:108 | ||||
| chr4:39698004-39698144 | Common:1; Rare:56 | ||||
| chr4:41990390-41990572 | Common:1; Rare:66 |