| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:7068017-7068385 | Common:7; Rare:126 | ||||
| chr4:8199042-8199333 | Common:2; Rare:76 | ||||
| chr4:8440713-8440790 | Rare:27 | ||||
| chr4:10116687-10117067 | Common:7; Rare:174 | ||||
| chr4:11428881-11429063 | Common:1; Rare:55 | ||||
| chr4:13627717-13627871 | Common:1; Rare:44 | ||||
| chr4:15655244-15655481 | Common:2; Rare:99 | ||||
| chr4:15681503-15681869 | Common:3; Rare:126 | ||||
| chr4:17577311-17577546 | Rare:110 | ||||
| chr4:17614548-17614716 | Common:3; Rare:102 | ||||
| chr4:17810687-17810891 | Rare:65 | ||||
| chr4:23890014-23890270 | Common:1; Rare:40 | ||||
| chr4:24912860-24913116 | Common:1; Rare:86 | ||||
| chr4:25160365-25160727 | Common:3; Rare:109; Clinvar:2; Clinvar (benign):1 | ||||
| chr4:25233824-25234058 | Rare:93 |