| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:25160376-25160727 | Common:3; Rare:101; Clinvar:2; Clinvar (benign):1 | ||||
| chr4:25914051-25914316 | Common:2; Rare:114 | ||||
| chr4:26320590-26320832 | Common:1; Rare:92 | ||||
| chr4:26320874-26321041 | Rare:56; Clinvar (benign):1 | ||||
| chr4:26860568-26860796 | Common:1; Rare:71 | ||||
| chr4:37826588-37826729 | Common:1; Rare:54 | ||||
| chr4:37977168-37977488 | Rare:78 | ||||
| chr4:38664205-38664306 | Rare:35 | ||||
| chr4:39458857-39459112 | Common:3; Rare:147; Clinvar (benign):5 | ||||
| chr4:39527363-39527761 | Common:2; Rare:97 | ||||
| chr4:39527941-39528034 | Rare:22 | ||||
| chr4:39638834-39639140 | Common:1; Rare:112 | ||||
| chr4:39697946-39698222 | Common:2; Rare:118 | ||||
| chr4:40629811-40630048 | Common:1; Rare:55 | ||||
| chr4:41990388-41990610 | Common:1; Rare:76 |