| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:30721978-30722163 | Common:1; Rare:61 | ||||
| chr4:36243840-36244034 | Common:1; Rare:40 | ||||
| chr4:36244290-36244593 | Common:3; Rare:104 | ||||
| chr4:37826571-37826765 | Common:1; Rare:74 | ||||
| chr4:38664214-38664443 | Common:1; Rare:68 | ||||
| chr4:38867606-38867833 | Common:2; Rare:82 | ||||
| chr4:38868060-38868115 | Rare:16 | ||||
| chr4:39182218-39182554 | Common:1; Rare:77; Clinvar:2; Clinvar (benign):1 | ||||
| chr4:39458843-39459122 | Common:3; Rare:158; Clinvar:1; Clinvar (benign):5 | ||||
| chr4:39527337-39527780 | Common:4; Rare:119 | ||||
| chr4:39527929-39528016 | Rare:20 | ||||
| chr4:39638834-39639190 | Common:1; Rare:134 | ||||
| chr4:39697936-39698241 | Common:2; Rare:127 | ||||
| chr4:39698353-39698378 | |||||
| chr4:39977339-39977636 | Common:2; Rare:84 |