| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:10026309-10026453 | Rare:49 | ||||
| chr3:11225865-11226020 | Rare:23 | ||||
| chr3:11643818-11643958 | Rare:42 | ||||
| chr3:11720475-11720867 | Common:1; Rare:79 | ||||
| chr3:12004284-12004358 | Common:1; Rare:20 | ||||
| chr3:12148441-12148504 | Common:1; Rare:11 | ||||
| chr3:12158708-12158721 | Rare:7 | ||||
| chr3:12158902-12159136 | Rare:70 | ||||
| chr3:12287747-12287970 | Common:6; Rare:39 | ||||
| chr3:12288958-12289080 | Common:1; Rare:24 | ||||
| chr3:12484361-12484554 | Common:2; Rare:60; Clinvar:3; Clinvar (benign):2 | ||||
| chr3:12664058-12664300 | Common:2; Rare:68; Clinvar:1; Clinvar (benign):4 | ||||
| chr3:13480040-13480334 | Common:2; Rare:69 | ||||
| chr3:14124728-14125173 | Common:4; Rare:126; Clinvar:4; Clinvar (benign):1 | ||||
| chr3:14178542-14178880 | Common:2; Rare:175; Clinvar:4; Clinvar (benign):1; Clinvar (pathogenic):1 |