| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:9769866-9770016 | Common:1; Rare:42 | ||||
| chr3:9792359-9793144 | Common:4; Rare:256 | ||||
| chr3:9933534-9933918 | Common:3; Rare:150; Clinvar:3 | ||||
| chr3:9952326-9952688 | Common:1; Rare:70 | ||||
| chr3:9978196-9978230 | Rare:8 | ||||
| chr3:9986635-9987172 | Common:5; Rare:158 | ||||
| chr3:10026300-10026484 | Rare:60 | ||||
| chr3:10115525-10115811 | Common:3; Rare:89 | ||||
| chr3:10141678-10141850 | Common:1; Rare:76; Clinvar:6; Clinvar (benign):17 | ||||
| chr3:11136815-11137271 | Rare:93 | ||||
| chr3:11137434-11137736 | Rare:60 | ||||
| chr3:11154391-11154542 | Common:3; Rare:40 | ||||
| chr3:11272176-11272427 | Common:2; Rare:62 | ||||
| chr3:11276891-11277098 | Rare:42 | ||||
| chr3:11643581-11644073 | Common:3; Rare:114 |