| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:15339830-15340008 | Rare:40 | ||||
| chr4:15655232-15655466 | Common:2; Rare:96 | ||||
| chr4:15681542-15681875 | Common:4; Rare:119 | ||||
| chr4:17614577-17614650 | Common:1; Rare:33 | ||||
| chr4:17810681-17811045 | Common:4; Rare:115 | ||||
| chr4:25160399-25160704 | Common:3; Rare:87; Clinvar:2; Clinvar (benign):1 | ||||
| chr4:25914051-25914292 | Common:2; Rare:103 | ||||
| chr4:26320590-26320832 | Common:1; Rare:92 | ||||
| chr4:26320874-26321041 | Rare:56; Clinvar (benign):1 | ||||
| chr4:37826576-37826724 | Common:1; Rare:55 | ||||
| chr4:38867693-38867826 | Common:1; Rare:56 | ||||
| chr4:39458857-39459065 | Common:3; Rare:116 | ||||
| chr4:39527359-39527754 | Common:2; Rare:93 | ||||
| chr4:39638847-39639209 | Common:1; Rare:140 | ||||
| chr4:39697989-39698203 | Common:1; Rare:88 |