| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:7939690-7940014 | Common:1; Rare:136 | ||||
| chr4:15655289-15655455 | Common:1; Rare:74 | ||||
| chr4:15681458-15681893 | Common:4; Rare:153 | ||||
| chr4:15702836-15703139 | Common:2; Rare:58 | ||||
| chr4:17614553-17614650 | Common:2; Rare:40 | ||||
| chr4:17810701-17811012 | Common:2; Rare:96 | ||||
| chr4:24795348-24795586 | Common:1; Rare:58 | ||||
| chr4:25160411-25160725 | Common:3; Rare:86; Clinvar:2; Clinvar (benign):1 | ||||
| chr4:25233853-25234050 | Rare:87 | ||||
| chr4:25914051-25914316 | Common:2; Rare:114 | ||||
| chr4:37826505-37826729 | Common:6; Rare:79 | ||||
| chr4:38867441-38867822 | Common:2; Rare:108 | ||||
| chr4:39182204-39182548 | Rare:74; Clinvar:2 | ||||
| chr4:39458857-39459065 | Common:3; Rare:116 | ||||
| chr4:39527400-39527719 | Common:2; Rare:76 |