| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:7787929-7788263 | Common:1; Rare:138 | ||||
| chr10:7818366-7818540 | Common:1; Rare:42 | ||||
| chr10:11164832-11165280 | Common:3; Rare:102 | ||||
| chr10:12043140-12043403 | Common:2; Rare:70 | ||||
| chr10:12129458-12129733 | Rare:111 | ||||
| chr10:12195817-12196261 | Rare:125 | ||||
| chr10:12349616-12349826 | Common:2; Rare:71 | ||||
| chr10:13099699-13099834 | Rare:33 | ||||
| chr10:13099952-13100273 | Common:4; Rare:78; Clinvar:3; Clinvar (benign):6 | ||||
| chr10:13300038-13300166 | Rare:49; Clinvar:1 | ||||
| chr10:13707172-13707332 | Common:2; Rare:28 | ||||
| chr10:14008103-14008409 | Rare:77 | ||||
| chr10:14008417-14008473 | Rare:11 | ||||
| chr10:14838029-14838395 | Common:2; Rare:103 | ||||
| chr10:14878606-14878891 | Common:2; Rare:91 |