| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:51983356-51983541 | Rare:39 | ||||
| chr3:51995848-51996052 | Common:3; Rare:74 | ||||
| chr3:52154378-52154521 | Common:1; Rare:38 | ||||
| chr3:52197964-52198171 | Common:1; Rare:87 | ||||
| chr3:52225557-52225726 | Rare:47 | ||||
| chr3:52239036-52239264 | Common:2; Rare:78 | ||||
| chr3:52245645-52246002 | Common:2; Rare:107 | ||||
| chr3:52246843-52247059 | Common:1; Rare:62 | ||||
| chr3:52278617-52278777 | Rare:57 | ||||
| chr3:52287749-52287863 | Common:2; Rare:49 | ||||
| chr3:52288018-52288085 | Rare:20 | ||||
| chr3:52403205-52403548 | Common:1; Rare:110; Clinvar:30; Clinvar (benign):19 | ||||
| chr3:52410393-52410684 | Rare:64 | ||||
| chr3:52455420-52455651 | Common:2; Rare:77 | ||||
| chr3:52479986-52480172 | Common:2; Rare:35 |