| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:30719951-30720102 | Common:1; Rare:27 | ||||
| chr4:30720161-30720611 | Common:4; Rare:110 | ||||
| chr4:37826538-37826729 | Common:6; Rare:68 | ||||
| chr4:37977157-37977453 | Rare:73 | ||||
| chr4:38856773-38856944 | Common:5; Rare:27 | ||||
| chr4:38867588-38867830 | Common:2; Rare:84 | ||||
| chr4:38868062-38868115 | Rare:16 | ||||
| chr4:39182202-39182552 | Common:1; Rare:78; Clinvar:2; Clinvar (benign):1 | ||||
| chr4:39366301-39366416 | Common:1; Rare:34 | ||||
| chr4:39458834-39459148 | Common:3; Rare:174; Clinvar:2; Clinvar (benign):5 | ||||
| chr4:39527331-39527780 | Common:4; Rare:119 | ||||
| chr4:39527916-39528043 | Rare:31 | ||||
| chr4:39638802-39639190 | Common:1; Rare:143 | ||||
| chr4:39697921-39698203 | Common:2; Rare:123 | ||||
| chr4:40056604-40056992 | Common:4; Rare:114 |