| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:14024615-14025063 | Common:7; Rare:184 | ||||
| chr10:14185070-14185680 | Common:44; Rare:469 | ||||
| chr10:14382051-14382370 | Common:2; Rare:72 | ||||
| chr10:14533430-14533830 | Common:6; Rare:117 | ||||
| chr10:14562762-14563936 | Common:12; Rare:229 | ||||
| chr10:14585562-14586140 | Common:7; Rare:149 | ||||
| chr10:14587942-14588496 | Common:8; Rare:217 | ||||
| chr10:14601442-14601842 | Common:5; Rare:71 | ||||
| chr10:14601830-14602356 | Common:5; Rare:213 | ||||
| chr10:14605341-14605580 | Common:2; Rare:41 | ||||
| chr10:14645130-14645590 | Common:5; Rare:132 | ||||
| chr10:14647930-14648580 | Common:7; Rare:187 | ||||
| chr10:14659520-14659740 | Common:5; Rare:35 | ||||
| chr10:14659650-14660150 | Common:11; Rare:166 | ||||
| chr10:14926800-14927001 | Common:2; Rare:65; Clinvar:1; Clinvar (benign):1 |