| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:16264866-16265243 | Common:2; Rare:128 | ||||
| chr3:19946974-19947457 | Common:7; Rare:179 | ||||
| chr3:21751020-21751413 | Common:4; Rare:122 | ||||
| chr3:23916911-23917181 | Rare:102 | ||||
| chr3:23917716-23917990 | Common:2; Rare:79; Clinvar (benign):1 | ||||
| chr3:25428107-25428357 | Rare:55 | ||||
| chr3:25790008-25790094 | Common:1; Rare:31 | ||||
| chr3:28348646-28348747 | Rare:24 | ||||
| chr3:28348779-28349182 | Common:3; Rare:128 | ||||
| chr3:29280851-29281092 | Common:3; Rare:45 | ||||
| chr3:30606226-30606521 | Common:1; Rare:65; Clinvar:1 | ||||
| chr3:31532383-31532656 | Common:4; Rare:76 | ||||
| chr3:32502763-32502960 | Rare:55 | ||||
| chr3:32570636-32571025 | Common:1; Rare:170 | ||||
| chr3:33218724-33219027 | Common:3; Rare:95 |