| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:93702388-93702690 | Common:5; Rare:102 | ||||
| chr10:93788589-93788644 | Common:1; Rare:7 | ||||
| chr10:93893872-93894097 | Common:1; Rare:88 | ||||
| chr10:94362899-94363027 | Common:3; Rare:51 | ||||
| chr10:94402312-94402502 | Rare:50 | ||||
| chr10:94545695-94546008 | Common:5; Rare:107 | ||||
| chr10:95290978-95291201 | Common:2; Rare:97 | ||||
| chr10:95482700-95482828 | Rare:15 | ||||
| chr10:95656619-95656783 | Common:1; Rare:53; Clinvar:5; Clinvar (benign):2 | ||||
| chr10:95656820-95656893 | Rare:13 | ||||
| chr10:95693836-95694249 | Common:5; Rare:135; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr10:95755656-95755747 | Rare:17 | ||||
| chr10:95755829-95756186 | Common:3; Rare:71 | ||||
| chr10:95907756-95907986 | Common:3; Rare:66 | ||||
| chr10:95908134-95908198 | Rare:17 |