| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:181261060-181261286 | Rare:78 | ||||
| chr6:693039-693188 | Rare:52 | ||||
| chr6:2971506-2971786 | Common:1; Rare:74 | ||||
| chr6:3118569-3118752 | Common:2; Rare:61 | ||||
| chr6:4021209-4021422 | Rare:99 | ||||
| chr6:5004006-5004061 | Rare:30 | ||||
| chr6:5260709-5261051 | Common:4; Rare:118; Clinvar (benign):2 | ||||
| chr6:7313102-7313298 | Common:5; Rare:76 | ||||
| chr6:7389740-7389875 | Common:1; Rare:40 | ||||
| chr6:8064320-8064581 | Common:4; Rare:88 | ||||
| chr6:8435361-8435648 | Common:3; Rare:101 | ||||
| chr6:10415034-10415180 | Common:1; Rare:49 | ||||
| chr6:10694607-10694988 | Common:4; Rare:101 | ||||
| chr6:10722839-10723224 | Common:6; Rare:129 | ||||
| chr6:10747582-10747881 | Common:3; Rare:111 |