| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:187291680-187292251 | Common:18; Rare:220 | ||||
| chr3:187737560-187738100 | Common:3; Rare:83 | ||||
| chr3:188153727-188154024 | Common:2; Rare:94 | ||||
| chr3:188154067-188154272 | Rare:116 | ||||
| chr3:188154260-188154770 | Common:2; Rare:241 | ||||
| chr3:188212377-188212734 | Common:1; Rare:54 | ||||
| chr3:190322347-190322552 | Common:3; Rare:85 | ||||
| chr3:190513850-190514137 | Common:4; Rare:147 | ||||
| chr3:191329230-191329647 | Common:7; Rare:217 | ||||
| chr3:192917824-192918003 | Common:4; Rare:152 | ||||
| chr3:193593096-193593385 | Rare:181; Clinvar:4; Clinvar (benign):4 | ||||
| chr3:194351282-194351448 | Rare:36 | ||||
| chr3:194486784-194487166 | Common:9; Rare:339 | ||||
| chr3:194633310-194633610 | Common:4; Rare:148 | ||||
| chr3:194633630-194633990 | Common:6; Rare:121 |