| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:27154281-27154480 | Rare:51 | ||||
| chr10:27155181-27155397 | Common:4; Rare:82; Clinvar:4; Clinvar (benign):4 | ||||
| chr10:27240545-27240637 | Common:2; Rare:23 | ||||
| chr10:27240711-27240895 | Rare:50 | ||||
| chr10:27241865-27242241 | Common:2; Rare:133 | ||||
| chr10:27504129-27504368 | Rare:125; Clinvar:4; Clinvar (benign):1 | ||||
| chr10:28532715-28532880 | Common:1; Rare:59 | ||||
| chr10:28533034-28533185 | Rare:60 | ||||
| chr10:28533222-28533582 | Common:1; Rare:145 | ||||
| chr10:28677245-28677526 | Common:5; Rare:130 | ||||
| chr10:29634863-29635071 | Rare:44 | ||||
| chr10:30059501-30059697 | Common:1; Rare:71 | ||||
| chr10:30433874-30434151 | Common:3; Rare:72 | ||||
| chr10:30434551-30434690 | Common:1; Rare:39 | ||||
| chr10:31031838-31032046 | Common:2; Rare:81 |