| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:51983404-51983541 | Rare:32 | ||||
| chr3:52197919-52198211 | Common:1; Rare:113 | ||||
| chr3:52239079-52239222 | Common:2; Rare:49 | ||||
| chr3:52287759-52287851 | Common:2; Rare:38 | ||||
| chr3:52452785-52453129 | Common:3; Rare:56 | ||||
| chr3:52455371-52455644 | Common:2; Rare:81 | ||||
| chr3:52685586-52686055 | Common:3; Rare:141 | ||||
| chr3:52705569-52706223 | Common:4; Rare:208 | ||||
| chr3:53347518-53347741 | Common:1; Rare:70 | ||||
| chr3:53891772-53892021 | Common:2; Rare:82 | ||||
| chr3:56557055-56557234 | Common:2; Rare:78 | ||||
| chr3:57227600-57227936 | Common:4; Rare:110 | ||||
| chr3:57556009-57556321 | Rare:75 | ||||
| chr3:57597306-57597669 | Common:4; Rare:114 | ||||
| chr3:57889883-57890099 | Rare:48; Clinvar (benign):2 |