| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:23857660-23857918 | Common:2; Rare:91 | ||||
| chr22:23894295-23894567 | Common:3; Rare:102 | ||||
| chr22:23974395-23974686 | Common:1; Rare:4 | ||||
| chr22:24270721-24270933 | Common:3; Rare:80 | ||||
| chr22:24271061-24271181 | Common:2; Rare:55 | ||||
| chr22:24555890-24556071 | Rare:53 | ||||
| chr22:25564677-25565004 | Common:1; Rare:132 | ||||
| chr22:26169316-26169735 | Common:2; Rare:112 | ||||
| chr22:26479522-26479606 | Rare:12 | ||||
| chr22:26483772-26483947 | Common:4; Rare:68; Clinvar:5; Clinvar (benign):1 | ||||
| chr22:26512397-26512552 | Common:1; Rare:65 | ||||
| chr22:26590077-26590220 | Common:3; Rare:58 | ||||
| chr22:27919195-27919538 | Common:5; Rare:155 | ||||
| chr22:28443180-28443443 | Rare:53 | ||||
| chr22:28741791-28742064 | Common:2; Rare:81; Clinvar:1; Clinvar (benign):3 |