| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:42079590-42079757 | Common:1; Rare:50 | ||||
| chr22:42090743-42090945 | Common:1; Rare:68 | ||||
| chr22:42614857-42615251 | Common:3; Rare:165 | ||||
| chr22:42649311-42649482 | Common:1; Rare:67 | ||||
| chr22:42720813-42720951 | Rare:44 | ||||
| chr22:43089356-43089506 | Common:3; Rare:46 | ||||
| chr22:43812279-43812441 | Common:2; Rare:56 | ||||
| chr22:43955261-43955562 | Common:4; Rare:88 | ||||
| chr22:44024156-44024329 | Common:1; Rare:59 | ||||
| chr22:45163777-45164008 | Common:2; Rare:83 | ||||
| chr22:45413594-45413717 | Rare:44 | ||||
| chr22:46053764-46053902 | Rare:53 | ||||
| chr22:46250257-46250393 | Common:2; Rare:38 | ||||
| chr22:46296589-46296977 | Common:2; Rare:121 | ||||
| chr22:46335621-46335760 | Common:2; Rare:57; Clinvar:4; Clinvar (benign):6 |