| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:52516561-52516730 | Rare:56 | ||||
| chr3:52685772-52686072 | Common:3; Rare:108 | ||||
| chr3:52705587-52706267 | Common:4; Rare:225 | ||||
| chr3:52770913-52771009 | Common:2; Rare:24 | ||||
| chr3:53347518-53347734 | Common:1; Rare:68 | ||||
| chr3:53891794-53891973 | Common:1; Rare:55 | ||||
| chr3:56557082-56557228 | Common:2; Rare:55 | ||||
| chr3:57079230-57079382 | Common:2; Rare:51 | ||||
| chr3:57227598-57227913 | Common:3; Rare:108 | ||||
| chr3:57555996-57556328 | Rare:82 | ||||
| chr3:57597280-57597677 | Common:4; Rare:125 | ||||
| chr3:57889883-57890129 | Rare:54; Clinvar (benign):2 | ||||
| chr3:58008243-58008445 | Common:2; Rare:75; Clinvar:1 | ||||
| chr3:58433782-58433939 | Rare:66; Clinvar:2; Clinvar (benign):3 | ||||
| chr3:58491793-58492159 | Common:3; Rare:92 |