| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:4493165-4493484 | Rare:115; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:8501620-8501937 | Common:2; Rare:120 | ||||
| chr3:9249617-9249742 | Common:1; Rare:34 | ||||
| chr3:9362971-9363098 | Common:1; Rare:46 | ||||
| chr3:9397428-9397679 | Rare:85 | ||||
| chr3:9749839-9750009 | Common:1; Rare:59 | ||||
| chr3:9792414-9792570 | Rare:40 | ||||
| chr3:9792732-9793119 | Common:3; Rare:133 | ||||
| chr3:9933503-9933857 | Common:2; Rare:142; Clinvar:3 | ||||
| chr3:10026334-10026465 | Rare:37 | ||||
| chr3:10141675-10141962 | Common:1; Rare:135; Clinvar:34; Clinvar (benign):28 | ||||
| chr3:12664087-12664321 | Common:1; Rare:64; Clinvar:1; Clinvar (benign):2 | ||||
| chr3:14124723-14125105 | Common:4; Rare:111; Clinvar:4; Clinvar (benign):1 | ||||
| chr3:14178569-14178870 | Common:2; Rare:155; Clinvar:4; Clinvar (benign):1 | ||||
| chr3:14402350-14402628 | Common:1; Rare:74 |