| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:37019411-37019856 | Common:5; Rare:130 | ||||
| chr22:37051556-37051776 | Common:2; Rare:60 | ||||
| chr22:37519352-37519415 | Rare:26 | ||||
| chr22:37608591-37609074 | Common:8; Rare:148 | ||||
| chr22:37675375-37675644 | Common:3; Rare:76 | ||||
| chr22:37696767-37697083 | Common:3; Rare:83 | ||||
| chr22:37746043-37746371 | Common:5; Rare:107; Clinvar (benign):1 | ||||
| chr22:37805146-37805455 | Common:4; Rare:114 | ||||
| chr22:37807640-37808033 | Common:4; Rare:143 | ||||
| chr22:37844306-37844610 | Common:1; Rare:86 | ||||
| chr22:37849263-37849485 | Rare:133 | ||||
| chr22:37906063-37906350 | Common:1; Rare:75 | ||||
| chr22:37953597-37953802 | Rare:81 | ||||
| chr22:38181704-38182053 | Common:3; Rare:94; Clinvar:1 | ||||
| chr22:38201786-38202000 | Rare:66 |