| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:10115523-10115748 | Common:3; Rare:82 | ||||
| chr3:10141650-10141962 | Common:3; Rare:142; Clinvar:34; Clinvar (benign):29 | ||||
| chr3:11154362-11154511 | Common:3; Rare:40 | ||||
| chr3:11225878-11226026 | Rare:19 | ||||
| chr3:11272219-11272428 | Common:2; Rare:48 | ||||
| chr3:11846834-11847008 | Common:1; Rare:50 | ||||
| chr3:12484371-12484517 | Common:1; Rare:42; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:12664081-12664330 | Common:1; Rare:68; Clinvar:1; Clinvar (benign):3 | ||||
| chr3:13480064-13480339 | Common:1; Rare:65 | ||||
| chr3:14124723-14125150 | Common:4; Rare:122; Clinvar:4; Clinvar (benign):1 | ||||
| chr3:14178524-14178881 | Common:2; Rare:185; Clinvar:5; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr3:14402462-14402621 | Rare:42 | ||||
| chr3:14651486-14651810 | Rare:94 | ||||
| chr3:14947244-14947554 | Common:3; Rare:143 | ||||
| chr3:15099122-15099304 | Rare:44 |