| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:35399905-35400199 | Rare:102 | ||||
| chr22:36239445-36239668 | Rare:78 | ||||
| chr22:36253019-36253213 | Rare:43 | ||||
| chr22:36387811-36388326 | Common:2; Rare:133; Clinvar:2; Clinvar (benign):1 | ||||
| chr22:36481548-36481734 | Common:2; Rare:52 | ||||
| chr22:36507015-36507176 | Common:3; Rare:55 | ||||
| chr22:36529080-36529533 | Common:6; Rare:142 | ||||
| chr22:36776030-36776377 | Common:2; Rare:86 | ||||
| chr22:36860842-36861203 | Common:2; Rare:80; Clinvar:1; Clinvar (benign):2 | ||||
| chr22:37019428-37019763 | Common:5; Rare:94 | ||||
| chr22:37199383-37199654 | Common:4; Rare:71 | ||||
| chr22:37244112-37244324 | Rare:56 | ||||
| chr22:37485976-37486298 | Rare:115 | ||||
| chr22:37486342-37486471 | Rare:45 | ||||
| chr22:37560320-37560540 | Common:1; Rare:72 |