| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:26583981-26584124 | Rare:28 | ||||
| chr4:26860560-26860785 | Rare:67 | ||||
| chr4:36281481-36281645 | Rare:28 | ||||
| chr4:37826579-37826729 | Common:1; Rare:55 | ||||
| chr4:37977152-37977459 | Rare:79 | ||||
| chr4:38664194-38664344 | Common:2; Rare:50 | ||||
| chr4:38867588-38867822 | Common:2; Rare:83 | ||||
| chr4:39182320-39182554 | Common:1; Rare:54; Clinvar:2; Clinvar (benign):1 | ||||
| chr4:39366324-39366456 | Rare:42 | ||||
| chr4:39458868-39459112 | Common:3; Rare:136; Clinvar (benign):5 | ||||
| chr4:39527314-39527775 | Common:6; Rare:122 | ||||
| chr4:39527952-39528021 | Rare:18 | ||||
| chr4:39638805-39639209 | Common:1; Rare:150 | ||||
| chr4:39697936-39698185 | Common:2; Rare:108 | ||||
| chr4:40056668-40056993 | Common:4; Rare:103 |