| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:123399355-123399653 | Common:1; Rare:91 | ||||
| chr4:127880811-127880939 | Rare:40 | ||||
| chr4:128061000-128061325 | Common:1; Rare:116 | ||||
| chr4:129093468-129093736 | Common:1; Rare:79 | ||||
| chr4:133149105-133149295 | Common:2; Rare:54 | ||||
| chr4:138242240-138242646 | Common:1; Rare:86 | ||||
| chr4:139084192-139084556 | Common:4; Rare:158 | ||||
| chr4:139301223-139301557 | Common:4; Rare:97 | ||||
| chr4:139302435-139302522 | Rare:23 | ||||
| chr4:139453683-139453749 | Common:2; Rare:21 | ||||
| chr4:139453766-139454225 | Common:3; Rare:128; Clinvar:10; Clinvar (benign):4 | ||||
| chr4:139556141-139556513 | Rare:74 | ||||
| chr4:140373393-140373701 | Common:2; Rare:127 | ||||
| chr4:143184853-143184998 | Common:5; Rare:55 | ||||
| chr4:143513846-143514078 | Common:2; Rare:104 |