| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:12042730-12042998 | Rare:69 | ||||
| chr10:12043125-12043561 | Common:3; Rare:122 | ||||
| chr10:12068592-12069081 | Common:2; Rare:170 | ||||
| chr10:12129328-12129750 | Common:1; Rare:156 | ||||
| chr10:12195764-12195990 | Rare:55 | ||||
| chr10:12196048-12196302 | Rare:82 | ||||
| chr10:12196431-12196594 | Rare:35 | ||||
| chr10:12348805-12349278 | Common:3; Rare:117 | ||||
| chr10:12349363-12349758 | Common:2; Rare:102 | ||||
| chr10:13099932-13100258 | Common:4; Rare:77; Clinvar:3; Clinvar (benign):6 | ||||
| chr10:13100585-13100695 | Common:1; Rare:20 | ||||
| chr10:13161252-13161643 | Common:1; Rare:108 | ||||
| chr10:13299538-13299722 | Common:1; Rare:39 | ||||
| chr10:13299977-13300240 | Rare:86; Clinvar:2 | ||||
| chr10:13302087-13302245 | Common:2; Rare:26 |