| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:121437632-121438032 | Common:5; Rare:66 | ||||
| chr10:121500119-121500519 | Common:4; Rare:126 | ||||
| chr10:121500550-121500890 | Rare:93; Clinvar (benign):2 | ||||
| chr10:121600720-121601140 | Common:6; Rare:78 | ||||
| chr10:121683770-121684150 | Common:4; Rare:67 | ||||
| chr10:121708543-121709290 | Common:11; Rare:148 | ||||
| chr10:121709333-121709733 | Common:4; Rare:107 | ||||
| chr10:121710250-121710356 | Rare:22 | ||||
| chr10:121921634-121921839 | Common:1; Rare:44 | ||||
| chr10:122044310-122044580 | Common:1; Rare:44 | ||||
| chr10:122063247-122063470 | Common:4; Rare:48 | ||||
| chr10:122113878-122115078 | Common:16; Rare:321 | ||||
| chr10:122139689-122140452 | Common:4; Rare:182 | ||||
| chr10:122164457-122164718 | Common:1; Rare:56 | ||||
| chr10:122164987-122165623 | Common:4; Rare:130 |