| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:41800545-41800691 | Common:1; Rare:42 | ||||
| chr22:41832909-41833149 | Common:3; Rare:80 | ||||
| chr22:42070802-42071003 | Common:3; Rare:44 | ||||
| chr22:42090740-42090945 | Common:1; Rare:71; Clinvar (pathogenic):1 | ||||
| chr22:42614870-42615246 | Common:3; Rare:151 | ||||
| chr22:42649333-42649481 | Common:1; Rare:57 | ||||
| chr22:43812302-43812437 | Common:1; Rare:48 | ||||
| chr22:43955291-43955560 | Common:3; Rare:79 | ||||
| chr22:45163766-45164003 | Common:2; Rare:92 | ||||
| chr22:46267832-46268030 | Common:1; Rare:58 | ||||
| chr22:46296679-46296918 | Common:2; Rare:86 | ||||
| chr22:46335643-46335760 | Common:1; Rare:48; Clinvar:4; Clinvar (benign):5 | ||||
| chr22:46762520-46762669 | Common:3; Rare:50 | ||||
| chr22:50783606-50783835 | Common:2; Rare:70 | ||||
| chr3:3126813-3126984 | Common:4; Rare:74; Clinvar (benign):1 |