| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:8501641-8501854 | Rare:75 | ||||
| chr3:9249627-9249742 | Common:1; Rare:33 | ||||
| chr3:9363004-9363098 | Rare:33 | ||||
| chr3:9397428-9397688 | Common:1; Rare:98 | ||||
| chr3:9749732-9749974 | Rare:78 | ||||
| chr3:9792414-9792523 | Rare:29 | ||||
| chr3:9792746-9793111 | Common:3; Rare:126 | ||||
| chr3:9933511-9933863 | Common:2; Rare:142; Clinvar:3 | ||||
| chr3:10026334-10026446 | Rare:33 | ||||
| chr3:12664084-12664330 | Common:1; Rare:67; Clinvar:1; Clinvar (benign):2 | ||||
| chr3:12840229-12840524 | Common:1; Rare:115 | ||||
| chr3:14124746-14125105 | Common:4; Rare:105; Clinvar:4; Clinvar (benign):1 | ||||
| chr3:14178573-14178858 | Common:2; Rare:147; Clinvar:3; Clinvar (benign):1 | ||||
| chr3:14402437-14402632 | Rare:48 | ||||
| chr3:14651486-14651828 | Rare:103 |