| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:19479116-19479465 | Common:4; Rare:125 | ||||
| chr22:19854791-19854997 | Rare:71 | ||||
| chr22:19941725-19942136 | Common:2; Rare:114; Clinvar:5; Clinvar (benign):4 | ||||
| chr22:20117123-20117616 | Common:3; Rare:157 | ||||
| chr22:20319981-20320202 | Common:2; Rare:79 | ||||
| chr22:20437808-20437997 | Rare:49 | ||||
| chr22:20495775-20495994 | Common:2; Rare:82 | ||||
| chr22:20858755-20859108 | Common:7; Rare:175; Clinvar:3; Clinvar (benign):5 | ||||
| chr22:20917182-20917490 | Rare:115 | ||||
| chr22:21002092-21002211 | Common:3; Rare:45 | ||||
| chr22:21642055-21642341 | Common:2; Rare:84 | ||||
| chr22:23894570-23894795 | Common:3; Rare:88 | ||||
| chr22:24555025-24555485 | Common:4; Rare:168 | ||||
| chr22:24555811-24556035 | Rare:74 | ||||
| chr22:24593037-24593197 | Common:1; Rare:47 |