| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:103966969-103967048 | Rare:25 | ||||
| chr10:104121742-104122174 | Common:3; Rare:143 | ||||
| chr10:104232309-104232534 | Common:1; Rare:58 | ||||
| chr10:104254642-104254935 | Common:3; Rare:62 | ||||
| chr10:104268912-104269208 | Common:3; Rare:73 | ||||
| chr10:104353559-104353612 | Common:1; Rare:11 | ||||
| chr10:109923404-109923661 | Common:2; Rare:94 | ||||
| chr10:109996371-109996395 | Rare:2 | ||||
| chr10:110005906-110005933 | Rare:7 | ||||
| chr10:110005945-110006108 | Common:3; Rare:44 | ||||
| chr10:110007683-110008086 | Common:1; Rare:117 | ||||
| chr10:110225885-110226185 | Common:1; Rare:80 | ||||
| chr10:110304857-110305121 | Common:2; Rare:91 | ||||
| chr10:110567391-110567804 | Common:2; Rare:124; Clinvar:2; Clinvar (benign):5 | ||||
| chr10:110567921-110567980 | Rare:12 |