| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:42857163-42857472 | Common:3; Rare:127 | ||||
| chr22:42959818-42959966 | Common:1; Rare:28 | ||||
| chr22:43015087-43015384 | Common:2; Rare:121 | ||||
| chr22:43143346-43143486 | Common:2; Rare:48 | ||||
| chr22:43812263-43812441 | Common:2; Rare:59 | ||||
| chr22:43955303-43955562 | Common:3; Rare:79 | ||||
| chr22:44024048-44024414 | Common:2; Rare:107 | ||||
| chr22:44312784-44313032 | Common:2; Rare:55 | ||||
| chr22:44668458-44668785 | Common:5; Rare:124 | ||||
| chr22:45163665-45164014 | Common:4; Rare:125 | ||||
| chr22:45309704-45309978 | Common:1; Rare:108 | ||||
| chr22:46053749-46053902 | Rare:58 | ||||
| chr22:46250254-46250438 | Common:3; Rare:62 | ||||
| chr22:46267870-46268042 | Common:1; Rare:56 | ||||
| chr22:46335601-46335760 | Common:2; Rare:68; Clinvar:7; Clinvar (benign):6 |