| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:9249617-9249757 | Common:1; Rare:36 | ||||
| chr3:9362965-9363098 | Common:1; Rare:48 | ||||
| chr3:9397428-9397679 | Rare:85 | ||||
| chr3:9749779-9750301 | Common:2; Rare:161 | ||||
| chr3:9792369-9792518 | Rare:46 | ||||
| chr3:9792726-9793040 | Common:1; Rare:100 | ||||
| chr3:9793070-9793123 | Common:1; Rare:27 | ||||
| chr3:9843968-9844103 | Common:2; Rare:59 | ||||
| chr3:9917055-9917147 | Common:1; Rare:17 | ||||
| chr3:9933663-9933863 | Common:1; Rare:76 | ||||
| chr3:10026334-10026484 | Rare:42 | ||||
| chr3:11154300-11154542 | Common:4; Rare:63 | ||||
| chr3:11272239-11272413 | Common:1; Rare:36 | ||||
| chr3:11720476-11720867 | Common:1; Rare:79 | ||||
| chr3:12484375-12484570 | Common:2; Rare:58; Clinvar:3; Clinvar (benign):2 |