| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:49929514-49929635 | Common:1; Rare:28 | ||||
| chr3:49929729-49930075 | Rare:108 | ||||
| chr3:49940374-49940441 | Rare:14 | ||||
| chr3:50088818-50089027 | Rare:56 | ||||
| chr3:50267405-50267720 | Common:3; Rare:92 | ||||
| chr3:50273006-50273156 | Rare:46 | ||||
| chr3:50292343-50292680 | Common:1; Rare:150 | ||||
| chr3:50299255-50299650 | Common:2; Rare:91 | ||||
| chr3:50322639-50322831 | Rare:32 | ||||
| chr3:50328173-50328349 | Rare:53 | ||||
| chr3:50350660-50350930 | Common:1; Rare:50 | ||||
| chr3:50351016-50351215 | Common:3; Rare:39 | ||||
| chr3:50365106-50365382 | Common:1; Rare:103; Clinvar:4; Clinvar (benign):1 | ||||
| chr3:50567600-50567860 | Common:1; Rare:80 | ||||
| chr3:50569421-50569602 | Common:1; Rare:40 |