| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:53130410-53130533 | Common:1; Rare:36; Clinvar (benign):2 | ||||
| chr3:53347504-53347730 | Common:2; Rare:74 | ||||
| chr3:53891794-53892021 | Common:2; Rare:71 | ||||
| chr3:54123433-54123519 | Rare:27 | ||||
| chr3:56557076-56557238 | Common:2; Rare:63 | ||||
| chr3:56801960-56802279 | Common:2; Rare:85 | ||||
| chr3:57227604-57227919 | Common:3; Rare:106 | ||||
| chr3:57555996-57556307 | Rare:76 | ||||
| chr3:57597331-57597744 | Common:4; Rare:123 | ||||
| chr3:57889750-57890090 | Common:1; Rare:65; Clinvar (benign):2 | ||||
| chr3:58433805-58433952 | Rare:57; Clinvar (benign):2 | ||||
| chr3:62318927-62319092 | Rare:66 | ||||
| chr3:62875325-62875707 | Common:4; Rare:85 | ||||
| chr3:63443192-63443367 | Rare:37 | ||||
| chr3:63863773-63864126 | Common:7; Rare:117 |