| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:100530133-100530210 | Rare:9 | ||||
| chr10:100535706-100536017 | Common:6; Rare:120 | ||||
| chr10:100912571-100912596 | Rare:4 | ||||
| chr10:100912612-100913040 | Common:1; Rare:121 | ||||
| chr10:100913283-100913438 | Common:1; Rare:52 | ||||
| chr10:100987395-100987606 | Common:1; Rare:80; Clinvar:1; Clinvar (benign):1 | ||||
| chr10:100996958-100997147 | Common:2; Rare:53 | ||||
| chr10:100997511-100997817 | Common:3; Rare:61 | ||||
| chr10:100997821-100997929 | Rare:23 | ||||
| chr10:100999165-100999362 | Common:3; Rare:33 | ||||
| chr10:100999633-100999721 | Common:1; Rare:22 | ||||
| chr10:101060940-101061559 | Common:2; Rare:162 | ||||
| chr10:101062609-101062875 | Common:3; Rare:92 | ||||
| chr10:101353753-101354220 | Common:1; Rare:143 | ||||
| chr10:101588092-101588385 | Rare:124; Clinvar:1 |