| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:37486375-37486449 | Rare:25 | ||||
| chr22:37560329-37560553 | Common:1; Rare:76 | ||||
| chr22:37608445-37608496 | Common:1; Rare:24 | ||||
| chr22:37608661-37609238 | Common:6; Rare:193 | ||||
| chr22:37609998-37610087 | Rare:20 | ||||
| chr22:37629789-37630055 | Common:2; Rare:70 | ||||
| chr22:37630681-37630961 | Common:1; Rare:71 | ||||
| chr22:37675349-37675710 | Common:4; Rare:103 | ||||
| chr22:37681568-37681746 | Common:1; Rare:36 | ||||
| chr22:37746076-37746412 | Common:3; Rare:105; Clinvar (benign):1 | ||||
| chr22:37807747-37808044 | Common:4; Rare:117 | ||||
| chr22:37843972-37844255 | Rare:84 | ||||
| chr22:37849293-37849481 | Rare:114 | ||||
| chr22:37849782-37850060 | Rare:86 | ||||
| chr22:37953507-37953797 | Common:1; Rare:104 |