| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:46762455-46762669 | Common:3; Rare:80 | ||||
| chr22:50185725-50185935 | Common:4; Rare:86 | ||||
| chr22:50244949-50245070 | Common:2; Rare:45 | ||||
| chr22:50326933-50327223 | Common:3; Rare:95 | ||||
| chr22:50562887-50563044 | Common:3; Rare:45 | ||||
| chr22:50628133-50628280 | Common:7; Rare:74; Clinvar:1 | ||||
| chr22:50783598-50783859 | Common:2; Rare:82 | ||||
| chr3:196415-196614 | Rare:51 | ||||
| chr3:196712-197029 | Common:2; Rare:102 | ||||
| chr3:197196-197352 | Rare:48 | ||||
| chr3:197503-198026 | Common:7; Rare:194 | ||||
| chr3:2098599-2098962 | Common:4; Rare:144 | ||||
| chr3:3126872-3126990 | Common:3; Rare:51; Clinvar (benign):2 | ||||
| chr3:3799865-3799877 | Rare:2 | ||||
| chr3:3799894-3799917 | Rare:6 |