| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:99659161-99659599 | Common:2; Rare:110 | ||||
| chr10:99732007-99732333 | Rare:122; Clinvar:4; Clinvar (benign):1 | ||||
| chr10:100009612-100009725 | Common:1; Rare:26 | ||||
| chr10:100009867-100010015 | Common:1; Rare:52 | ||||
| chr10:100185866-100186400 | Common:2; Rare:154 | ||||
| chr10:100229526-100229728 | Common:1; Rare:72 | ||||
| chr10:100267278-100267340 | Common:1; Rare:16 | ||||
| chr10:100267539-100267876 | Common:4; Rare:105 | ||||
| chr10:100286088-100286474 | Rare:85 | ||||
| chr10:100286594-100286850 | Common:5; Rare:114 | ||||
| chr10:100346481-100346711 | Common:4; Rare:52 | ||||
| chr10:100346889-100347402 | Common:1; Rare:114 | ||||
| chr10:100528916-100529117 | Rare:32 | ||||
| chr10:100529788-100530033 | Common:1; Rare:74 | ||||
| chr10:100535709-100536056 | Common:6; Rare:131 |