| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:15655289-15655595 | Common:1; Rare:141 | ||||
| chr4:15681557-15681757 | Common:3; Rare:63 | ||||
| chr4:15703007-15703119 | Common:1; Rare:22 | ||||
| chr4:16083260-16083627 | Common:4; Rare:89 | ||||
| chr4:16083667-16083877 | Common:2; Rare:62 | ||||
| chr4:16083902-16083948 | Common:1; Rare:11 | ||||
| chr4:17614581-17614730 | Common:2; Rare:98 | ||||
| chr4:17810696-17810988 | Common:1; Rare:89 | ||||
| chr4:25160378-25160727 | Common:3; Rare:100; Clinvar:2; Clinvar (benign):1 | ||||
| chr4:25233841-25234104 | Rare:106 | ||||
| chr4:25312515-25312823 | Common:2; Rare:95 | ||||
| chr4:25914051-25914275 | Common:2; Rare:98 | ||||
| chr4:26320904-26321041 | Rare:48; Clinvar (benign):1 | ||||
| chr4:26857414-26857749 | Common:4; Rare:87 | ||||
| chr4:26860565-26860846 | Common:3; Rare:97 |