| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:16884851-16885260 | Common:7; Rare:100 | ||||
| chr3:17742500-17742767 | Common:3; Rare:87 | ||||
| chr3:18424197-18424565 | Common:5; Rare:72 | ||||
| chr3:19946974-19947503 | Common:7; Rare:194 | ||||
| chr3:20186148-20186518 | Common:6; Rare:116 | ||||
| chr3:21751062-21751415 | Common:4; Rare:112 | ||||
| chr3:23202918-23203200 | Common:1; Rare:99 | ||||
| chr3:23916870-23917214 | Rare:135 | ||||
| chr3:23917666-23918041 | Common:2; Rare:98; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:24494126-24494419 | Common:1; Rare:63 | ||||
| chr3:24494736-24494903 | Rare:44 | ||||
| chr3:24494927-24495289 | Common:3; Rare:97 | ||||
| chr3:25428106-25428402 | Rare:66 | ||||
| chr3:25664777-25665031 | Common:4; Rare:63 | ||||
| chr3:25783371-25783621 | Common:2; Rare:88; Clinvar (benign):3 |