| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:37243818-37243977 | Common:2; Rare:36 | ||||
| chr4:37826472-37826729 | Common:7; Rare:86 | ||||
| chr4:37977133-37977447 | Rare:82 | ||||
| chr4:38867490-38867814 | Common:2; Rare:98 | ||||
| chr4:39182171-39182548 | Rare:85; Clinvar:2 | ||||
| chr4:39366253-39366419 | Common:1; Rare:53 | ||||
| chr4:39458843-39459123 | Common:3; Rare:159; Clinvar:1; Clinvar (benign):5 | ||||
| chr4:39527337-39527780 | Common:4; Rare:119 | ||||
| chr4:39527944-39528021 | Rare:18 | ||||
| chr4:39638829-39639209 | Common:1; Rare:146 | ||||
| chr4:39697929-39698235 | Common:2; Rare:129 | ||||
| chr4:39977339-39977638 | Common:2; Rare:85 | ||||
| chr4:39977802-39978099 | Common:2; Rare:89 | ||||
| chr4:40056607-40057030 | Common:4; Rare:123 | ||||
| chr4:40335323-40335449 | Rare:33 |