| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:12616417-12616602 | Common:2; Rare:35 | ||||
| chr1:12617202-12617508 | Rare:81 | ||||
| chr1:12617673-12617881 | Common:5; Rare:17 | ||||
| chr1:12618093-12618475 | Common:3; Rare:84 | ||||
| chr1:15526553-15526924 | Common:2; Rare:120 | ||||
| chr1:15617215-15617447 | Common:1; Rare:69 | ||||
| chr1:16352397-16352569 | Common:2; Rare:98 | ||||
| chr1:16613486-16613844 | Common:6; Rare:1 | ||||
| chr1:17054102-17054394 | Common:1; Rare:72; Clinvar:1; Clinvar (benign):2 | ||||
| chr1:19095636-19095754 | Common:1; Rare:27 | ||||
| chr1:19210238-19210515 | Rare:93 | ||||
| chr1:19251502-19251854 | Common:6; Rare:117 | ||||
| chr1:19288766-19288865 | Common:1; Rare:33 | ||||
| chr1:19312012-19312350 | Common:8; Rare:158 | ||||
| chr1:19485439-19485737 | Common:1; Rare:99 |