| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:97633431-97633610 | Common:2; Rare:44 | ||||
| chr10:97713434-97713478 | Rare:13 | ||||
| chr10:98134537-98134688 | Common:1; Rare:54 | ||||
| chr10:98268188-98268458 | Common:3; Rare:69 | ||||
| chr10:98425651-98425885 | Common:1; Rare:62; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr10:99430613-99430994 | Common:3; Rare:92 | ||||
| chr10:99659239-99659547 | Common:1; Rare:79 | ||||
| chr10:99732072-99732335 | Rare:97; Clinvar:4 | ||||
| chr10:100185888-100186198 | Rare:113 | ||||
| chr10:100229553-100229664 | Rare:38 | ||||
| chr10:100286343-100286721 | Common:4; Rare:138 | ||||
| chr10:100346921-100347531 | Common:4; Rare:145 | ||||
| chr10:100529844-100530006 | Common:1; Rare:43 | ||||
| chr10:100912751-100913074 | Common:1; Rare:98 | ||||
| chr10:100913335-100913359 | Rare:8 |