| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:42160063-42160305 | Common:4; Rare:82 | ||||
| chr3:42502401-42502656 | Common:1; Rare:58 | ||||
| chr3:42581900-42582204 | Common:6; Rare:165 | ||||
| chr3:42582230-42582560 | Common:3; Rare:68 | ||||
| chr3:42590560-42590989 | Common:8; Rare:242 | ||||
| chr3:42600297-42600773 | Common:6; Rare:355 | ||||
| chr3:42600865-42601015 | Rare:96 | ||||
| chr3:42654160-42654690 | Common:4; Rare:232 | ||||
| chr3:42804369-42804712 | Common:4; Rare:193 | ||||
| chr3:42875818-42876006 | Rare:39 | ||||
| chr3:43621908-43622331 | Common:4; Rare:240; Clinvar:14; Clinvar (benign):2 | ||||
| chr3:43690799-43691089 | Common:6; Rare:212; Clinvar:14; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr3:43691499-43691770 | Common:3; Rare:91 | ||||
| chr3:44338057-44338187 | Common:4; Rare:88 | ||||
| chr3:44338200-44338580 | Common:6; Rare:169 |