| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:193240980-193241327 | Common:4; Rare:118 | ||||
| chr3:193593088-193593404 | Rare:98; Clinvar:2; Clinvar (benign):2 | ||||
| chr3:194672153-194672482 | Common:2; Rare:99 | ||||
| chr3:194672513-194672625 | Rare:26 | ||||
| chr3:195356157-195356332 | Rare:48 | ||||
| chr3:195442362-195442420 | Rare:18 | ||||
| chr3:195543188-195543475 | Common:3; Rare:102 | ||||
| chr3:195583882-195584194 | Common:9; Rare:71 | ||||
| chr3:195895922-195895990 | Rare:28 | ||||
| chr3:196082048-196082259 | Common:2; Rare:86 | ||||
| chr3:196287657-196287841 | Common:1; Rare:61 | ||||
| chr3:196318184-196318378 | Common:1; Rare:76 | ||||
| chr3:196432383-196432550 | Common:1; Rare:74 | ||||
| chr3:196503619-196503921 | Common:5; Rare:101 | ||||
| chr3:196568512-196568851 | Common:5; Rare:105 |