| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:12043126-12043511 | Common:2; Rare:107 | ||||
| chr10:12068683-12069057 | Common:2; Rare:137 | ||||
| chr10:12129391-12129729 | Rare:133 | ||||
| chr10:12195804-12196268 | Rare:133 | ||||
| chr10:12349154-12349273 | Rare:33 | ||||
| chr10:12349372-12349619 | Common:1; Rare:57 | ||||
| chr10:13001711-13001944 | Common:1; Rare:62 | ||||
| chr10:13099733-13100130 | Common:2; Rare:96; Clinvar:1; Clinvar (benign):2 | ||||
| chr10:13161246-13161603 | Common:1; Rare:95 | ||||
| chr10:13299420-13299880 | Common:7; Rare:97 | ||||
| chr10:13299977-13300210 | Rare:80; Clinvar:2 | ||||
| chr10:13301910-13302210 | Common:1; Rare:70 | ||||
| chr10:13302271-13302597 | Rare:66 | ||||
| chr10:13348231-13348438 | Rare:55 | ||||
| chr10:13528858-13529156 | Common:1; Rare:78 |