| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:40457207-40457370 | Common:2; Rare:78 | ||||
| chr3:40505775-40506132 | Rare:85 | ||||
| chr3:40524795-40524964 | Common:1; Rare:44 | ||||
| chr3:41962053-41962365 | Common:4; Rare:74 | ||||
| chr3:42160050-42160245 | Common:1; Rare:37 | ||||
| chr3:42581900-42582188 | Common:3; Rare:86 | ||||
| chr3:42590645-42590958 | Common:3; Rare:95 | ||||
| chr3:42600372-42600757 | Common:2; Rare:149 | ||||
| chr3:42600890-42601000 | Rare:42 | ||||
| chr3:42804434-42804671 | Common:2; Rare:74 | ||||
| chr3:43621914-43622312 | Common:2; Rare:116; Clinvar:7; Clinvar (benign):1 | ||||
| chr3:43690754-43690939 | Common:1; Rare:83; Clinvar:5; Clinvar (benign):1 | ||||
| chr3:44338057-44338173 | Common:2; Rare:38 | ||||
| chr3:44338319-44338458 | Common:2; Rare:48 | ||||
| chr3:44338675-44338800 | Common:3; Rare:47 |