| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:49017708-49017814 | Rare:36 | ||||
| chr3:49018288-49018462 | Common:1; Rare:53 | ||||
| chr3:49018481-49018697 | Common:1; Rare:86 | ||||
| chr3:49020269-49020548 | Common:1; Rare:50 | ||||
| chr3:49021295-49021852 | Common:2; Rare:142; Clinvar:3; Clinvar (benign):1 | ||||
| chr3:49021952-49022240 | Rare:96; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr3:49029246-49029573 | Common:2; Rare:201 | ||||
| chr3:49093425-49093509 | Rare:17 | ||||
| chr3:49093601-49093685 | Common:1; Rare:31 | ||||
| chr3:49093952-49094458 | Common:1; Rare:125 | ||||
| chr3:49104445-49104619 | Rare:65; Clinvar:4; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr3:49104629-49104985 | Common:1; Rare:140; Clinvar:3; Clinvar (benign):7 | ||||
| chr3:49120702-49121069 | Rare:106 | ||||
| chr3:49166257-49166491 | Common:1; Rare:55 | ||||
| chr3:49171148-49171249 | Rare:19 |