| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:97633424-97633627 | Common:2; Rare:54 | ||||
| chr10:97687372-97687663 | Common:3; Rare:81 | ||||
| chr10:98268183-98268442 | Common:3; Rare:67 | ||||
| chr10:98446850-98446967 | Rare:31; Clinvar:1 | ||||
| chr10:99235650-99236263 | Common:5; Rare:171; Clinvar (pathogenic):1 | ||||
| chr10:99430616-99430965 | Common:3; Rare:85 | ||||
| chr10:99659256-99659556 | Common:1; Rare:74 | ||||
| chr10:99732072-99732344 | Rare:102; Clinvar:4 | ||||
| chr10:100185920-100186152 | Rare:87 | ||||
| chr10:100229551-100229625 | Rare:21 | ||||
| chr10:100286343-100286451 | Rare:23 | ||||
| chr10:100286661-100286730 | Rare:31 | ||||
| chr10:100347266-100347357 | Rare:15 | ||||
| chr10:100529803-100530006 | Common:1; Rare:61 | ||||
| chr10:100912736-100913031 | Common:1; Rare:91 |