| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:23868252-23868518 | Common:6; Rare:74; Clinvar:2; Clinvar (benign):5 | ||||
| chr1:23959035-23959299 | Common:3; Rare:50 | ||||
| chr1:23959608-23959877 | Common:2; Rare:74 | ||||
| chr1:23980189-23980604 | Common:1; Rare:114 | ||||
| chr1:24413684-24413855 | Common:1; Rare:39 | ||||
| chr1:24502749-24503057 | Common:2; Rare:88 | ||||
| chr1:24642911-24643354 | Common:2; Rare:144 | ||||
| chr1:24745034-24745556 | Common:5; Rare:183 | ||||
| chr1:25232428-25232707 | Rare:108 | ||||
| chr1:25247056-25247125 | Rare:18 | ||||
| chr1:25247445-25247639 | Common:2; Rare:69 | ||||
| chr1:25338208-25338447 | Common:1; Rare:83 | ||||
| chr1:25819858-25820021 | Common:2; Rare:51 | ||||
| chr1:25859343-25859611 | Common:3; Rare:114 | ||||
| chr1:25998126-25998448 | Common:3; Rare:83 |