| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:52685942-52686104 | Common:2; Rare:69 | ||||
| chr3:52705558-52706223 | Common:4; Rare:212 | ||||
| chr3:52770921-52771019 | Common:2; Rare:22 | ||||
| chr3:53130387-53130561 | Common:1; Rare:61; Clinvar:1; Clinvar (benign):3 | ||||
| chr3:53255924-53256169 | Common:3; Rare:94 | ||||
| chr3:53347518-53347741 | Common:1; Rare:70 | ||||
| chr3:53882061-53882418 | Common:4; Rare:115 | ||||
| chr3:53891807-53892034 | Common:2; Rare:68 | ||||
| chr3:55481023-55481173 | Rare:27 | ||||
| chr3:55487518-55487664 | Rare:30; Clinvar:3 | ||||
| chr3:56557076-56557226 | Common:2; Rare:56 | ||||
| chr3:57079269-57079434 | Common:2; Rare:55 | ||||
| chr3:57227592-57227911 | Common:3; Rare:111 | ||||
| chr3:57555981-57556343 | Rare:94 | ||||
| chr3:57597294-57597778 | Common:4; Rare:142 |