| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:37242958-37243429 | Common:5; Rare:122 | ||||
| chr3:38024510-38024652 | Common:1; Rare:52 | ||||
| chr3:38454658-38454722 | Common:1; Rare:12 | ||||
| chr3:39051944-39052038 | Common:1; Rare:35 | ||||
| chr3:39153539-39153750 | Common:3; Rare:66 | ||||
| chr3:39383319-39383694 | Common:3; Rare:87; Clinvar:7; Clinvar (benign):2 | ||||
| chr3:40309491-40309838 | Common:9; Rare:120 | ||||
| chr3:40505967-40506115 | Rare:29 | ||||
| chr3:40524833-40524911 | Common:1; Rare:17 | ||||
| chr3:42159937-42160222 | Common:1; Rare:55 | ||||
| chr3:42581898-42582137 | Common:3; Rare:75 | ||||
| chr3:42600355-42600749 | Common:3; Rare:158 | ||||
| chr3:42685369-42685588 | Rare:50 | ||||
| chr3:42701518-42701669 | Common:1; Rare:23 | ||||
| chr3:42702588-42702755 | Rare:40 |