| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:19946974-19947415 | Common:5; Rare:166 | ||||
| chr3:23202930-23203220 | Common:1; Rare:101 | ||||
| chr3:23916880-23917177 | Rare:112 | ||||
| chr3:23917648-23917989 | Common:2; Rare:90; Clinvar (benign):1 | ||||
| chr3:24494304-24494325 | Rare:2 | ||||
| chr3:24495163-24495384 | Common:4; Rare:54 | ||||
| chr3:25428094-25428391 | Rare:66 | ||||
| chr3:25664882-25665063 | Common:1; Rare:58 | ||||
| chr3:25783388-25783627 | Common:2; Rare:79; Clinvar (benign):3 | ||||
| chr3:25790008-25790118 | Common:3; Rare:42 | ||||
| chr3:27369236-27369614 | Common:1; Rare:90 | ||||
| chr3:28348644-28348741 | Rare:21 | ||||
| chr3:28348784-28349196 | Common:4; Rare:130 | ||||
| chr3:29280852-29281081 | Common:3; Rare:43 | ||||
| chr3:30606561-30606957 | Common:1; Rare:123; Clinvar:7; Clinvar (benign):5 |