| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:52277693-52277837 | Common:1; Rare:41 | ||||
| chr3:52278611-52278801 | Rare:69 | ||||
| chr3:52287759-52287871 | Common:2; Rare:46 | ||||
| chr3:52288012-52288085 | Rare:23 | ||||
| chr3:52317836-52317894 | Rare:17 | ||||
| chr3:52403865-52404034 | Rare:40; Clinvar:5; Clinvar (benign):5 | ||||
| chr3:52409909-52410061 | Rare:45 | ||||
| chr3:52410449-52411337 | Common:2; Rare:199 | ||||
| chr3:52412597-52412938 | Common:3; Rare:87 | ||||
| chr3:52455086-52455150 | Rare:9 | ||||
| chr3:52455406-52455758 | Common:2; Rare:109 | ||||
| chr3:52484247-52484636 | Common:8; Rare:106 | ||||
| chr3:52525207-52525385 | Rare:64 | ||||
| chr3:52532313-52532595 | Common:1; Rare:47 | ||||
| chr3:52534643-52534870 | Common:1; Rare:47 |