| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:110226096-110226272 | Common:1; Rare:47 | ||||
| chr10:110226309-110226371 | Rare:20 | ||||
| chr10:110227024-110227351 | Common:2; Rare:25 | ||||
| chr10:110304812-110305260 | Common:2; Rare:131 | ||||
| chr10:110305291-110305421 | Common:1; Rare:29 | ||||
| chr10:110497400-110497492 | Rare:21 | ||||
| chr10:110497648-110497995 | Common:5; Rare:122 | ||||
| chr10:110498159-110498312 | Common:1; Rare:74 | ||||
| chr10:110567095-110567830 | Common:4; Rare:230; Clinvar:2; Clinvar (benign):5 | ||||
| chr10:110567896-110567990 | Common:2; Rare:20 | ||||
| chr10:110568195-110568586 | Common:5; Rare:96 | ||||
| chr10:110871561-110872083 | Rare:165 | ||||
| chr10:110872178-110872499 | Rare:91 | ||||
| chr10:110918440-110918818 | Common:3; Rare:105 | ||||
| chr10:110918914-110919660 | Common:8; Rare:192; Clinvar:1; Clinvar (benign):1 |