| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:50623214-50623536 | Common:3; Rare:127 | ||||
| chr10:50623762-50624158 | Common:5; Rare:315 | ||||
| chr10:50624483-50625090 | Common:17; Rare:421 | ||||
| chr10:50625131-50625364 | Common:4; Rare:117 | ||||
| chr10:50739771-50740019 | Common:1; Rare:117 | ||||
| chr10:50740050-50740370 | Common:5; Rare:84 | ||||
| chr10:50990842-50991381 | Common:11; Rare:162 | ||||
| chr10:50991420-50991690 | Common:3; Rare:109 | ||||
| chr10:51074220-51074600 | Common:4; Rare:140; Clinvar (benign):4 | ||||
| chr10:51074544-51074944 | Common:1; Rare:158; Clinvar:1; Clinvar (benign):16 | ||||
| chr10:51699522-51700007 | Common:13; Rare:257 | ||||
| chr10:52313601-52314375 | Common:10; Rare:352 | ||||
| chr10:52314360-52314782 | Rare:191 | ||||
| chr10:52315010-52315350 | Common:4; Rare:141 | ||||
| chr10:56361196-56361554 | Common:20; Rare:333 |