| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:186930489-186930765 | Common:2; Rare:72 | ||||
| chr3:187139433-187139594 | Rare:63 | ||||
| chr3:187291687-187291891 | Common:1; Rare:70 | ||||
| chr3:188153791-188153986 | Common:1; Rare:36 | ||||
| chr3:188154046-188154230 | Rare:61 | ||||
| chr3:188947662-188947819 | Common:1; Rare:57 | ||||
| chr3:191329302-191329632 | Common:3; Rare:94 | ||||
| chr3:192917827-192918003 | Common:2; Rare:79 | ||||
| chr3:193554859-193554904 | Rare:7 | ||||
| chr3:193593088-193593394 | Rare:97; Clinvar:2; Clinvar (benign):2 | ||||
| chr3:194486967-194487165 | Common:4; Rare:95 | ||||
| chr3:195543215-195543449 | Common:3; Rare:89 | ||||
| chr3:195583876-195584056 | Rare:35 | ||||
| chr3:195584103-195584410 | Common:12; Rare:61 | ||||
| chr3:196082068-196082247 | Common:2; Rare:69 |