| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:49007790-49008046 | Common:2; Rare:69 | ||||
| chr3:49018505-49018611 | Rare:47 | ||||
| chr3:49020981-49021099 | Rare:27 | ||||
| chr3:49021498-49021765 | Rare:60; Clinvar:1 | ||||
| chr3:49022020-49022373 | Rare:135; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr3:49022500-49022768 | Common:1; Rare:102; Clinvar:2; Clinvar (benign):2 | ||||
| chr3:49025149-49025446 | Common:1; Rare:63 | ||||
| chr3:49028290-49028491 | Rare:63 | ||||
| chr3:49029314-49029557 | Common:2; Rare:162 | ||||
| chr3:49093422-49093676 | Common:1; Rare:88 | ||||
| chr3:49104608-49104948 | Common:1; Rare:134; Clinvar:5; Clinvar (benign):7 | ||||
| chr3:49105060-49105212 | Rare:26 | ||||
| chr3:49120747-49120861 | Rare:33 | ||||
| chr3:49120868-49120979 | Rare:35 | ||||
| chr3:49121721-49122050 | Common:2; Rare:103; Clinvar:4; Clinvar (benign):5 |