| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:19485082-19485104 | Rare:8 | ||||
| chr22:19505938-19506011 | Rare:13 | ||||
| chr22:19666676-19667008 | Common:3; Rare:61 | ||||
| chr22:19758639-19758816 | Rare:53 | ||||
| chr22:19759731-19760354 | Common:9; Rare:133 | ||||
| chr22:19853446-19853746 | Rare:77 | ||||
| chr22:19877072-19877505 | Common:1; Rare:135; Clinvar:3; Clinvar (benign):5 | ||||
| chr22:19878035-19878416 | Common:2; Rare:120; Clinvar:6; Clinvar (benign):6; Clinvar (pathogenic):1 | ||||
| chr22:19878870-19879257 | Common:1; Rare:87 | ||||
| chr22:19879376-19879556 | Common:2; Rare:42 | ||||
| chr22:19881890-19882161 | Common:3; Rare:44 | ||||
| chr22:19887001-19887394 | Common:3; Rare:66 | ||||
| chr22:19891872-19892179 | Common:2; Rare:86 | ||||
| chr22:19892424-19892802 | Common:2; Rare:90 | ||||
| chr22:19942542-19942825 | Common:5; Rare:54 |