| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:52455430-52455638 | Common:2; Rare:70 | ||||
| chr3:52685952-52686108 | Common:2; Rare:68 | ||||
| chr3:52704832-52705091 | Rare:40 | ||||
| chr3:52705548-52706252 | Common:4; Rare:228 | ||||
| chr3:53130387-53130517 | Common:1; Rare:49; Clinvar:1; Clinvar (benign):3 | ||||
| chr3:53347518-53347728 | Common:1; Rare:66 | ||||
| chr3:53891802-53892021 | Common:2; Rare:70 | ||||
| chr3:57227604-57227899 | Common:3; Rare:101 | ||||
| chr3:57556032-57556307 | Rare:67 | ||||
| chr3:57597326-57597668 | Common:4; Rare:107 | ||||
| chr3:62318890-62319058 | Rare:71 | ||||
| chr3:63863777-63864137 | Common:7; Rare:121 | ||||
| chr3:66038764-66039064 | Common:3; Rare:109 | ||||
| chr3:67654583-67654722 | Common:1; Rare:48 | ||||
| chr3:69013178-69013330 | Rare:40 |