| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:37977212-37977480 | Rare:63 | ||||
| chr4:38664189-38664410 | Common:2; Rare:68 | ||||
| chr4:38664835-38665024 | Rare:62 | ||||
| chr4:38867565-38867822 | Common:2; Rare:87 | ||||
| chr4:38867979-38868115 | Common:1; Rare:37 | ||||
| chr4:39182347-39182554 | Common:1; Rare:49; Clinvar:2; Clinvar (benign):1 | ||||
| chr4:39366319-39366431 | Rare:35 | ||||
| chr4:39458857-39459122 | Common:3; Rare:153; Clinvar:1; Clinvar (benign):5 | ||||
| chr4:39527337-39527801 | Common:4; Rare:129 | ||||
| chr4:39527892-39528070 | Rare:37 | ||||
| chr4:39638651-39639169 | Common:1; Rare:162 | ||||
| chr4:39697997-39698318 | Common:1; Rare:115 | ||||
| chr4:39698334-39698378 | Rare:3 | ||||
| chr4:40056584-40056944 | Common:4; Rare:112 | ||||
| chr4:40057210-40057268 | Common:1; Rare:19 |