| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:52495300-52495435 | Rare:44 | ||||
| chr3:52516561-52516730 | Rare:56 | ||||
| chr3:52525056-52525330 | Common:8; Rare:123 | ||||
| chr3:52536360-52536756 | Common:3; Rare:129 | ||||
| chr3:52685593-52685914 | Common:2; Rare:90 | ||||
| chr3:52685937-52686202 | Common:2; Rare:101 | ||||
| chr3:52693187-52693480 | Common:4; Rare:88 | ||||
| chr3:52705569-52706257 | Common:4; Rare:224 | ||||
| chr3:52770911-52771022 | Common:2; Rare:25 | ||||
| chr3:52794679-52794806 | Rare:39 | ||||
| chr3:52802125-52802239 | Common:1; Rare:28 | ||||
| chr3:53130396-53130509 | Rare:43; Clinvar:1; Clinvar (benign):3 | ||||
| chr3:53347504-53347734 | Common:2; Rare:74 | ||||
| chr3:53891794-53892017 | Common:2; Rare:70 | ||||
| chr3:55487652-55487704 | Common:3; Rare:10 |