| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:40453155-40453417 | Common:6; Rare:58 | ||||
| chr3:41225308-41225819 | Rare:106; Clinvar:1; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr3:41237751-41238070 | Common:1; Rare:82; Clinvar (pathogenic):1 | ||||
| chr3:42216377-42216442 | Rare:15 | ||||
| chr3:42800983-42801199 | Common:1; Rare:35 | ||||
| chr3:45007234-45007429 | Common:2; Rare:51 | ||||
| chr3:46998884-46999063 | Common:1; Rare:60; Clinvar:1 | ||||
| chr3:47164778-47164896 | Common:2; Rare:24 | ||||
| chr3:47406096-47406367 | Common:1; Rare:62; Clinvar (benign):1 | ||||
| chr3:47412319-47412591 | Rare:98 | ||||
| chr3:50358428-50358613 | Rare:61 | ||||
| chr3:52277604-52277780 | Rare:45 | ||||
| chr3:52550753-52551026 | Common:1; Rare:57 | ||||
| chr3:53156522-53156835 | Common:4; Rare:74 | ||||
| chr3:53864120-53864231 | Common:1; Rare:15 |