| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:41224722-41225032 | Common:1; Rare:65; Clinvar (pathogenic):2 | ||||
| chr3:41962022-41962370 | Common:5; Rare:88 | ||||
| chr3:42160131-42160304 | Common:2; Rare:38 | ||||
| chr3:42581848-42582123 | Common:3; Rare:89 | ||||
| chr3:42582277-42582428 | Common:1; Rare:37 | ||||
| chr3:42600314-42601035 | Common:3; Rare:259 | ||||
| chr3:42631042-42631316 | Rare:50 | ||||
| chr3:42643949-42644069 | Rare:36 | ||||
| chr3:42653376-42653739 | Rare:71 | ||||
| chr3:42773206-42773348 | Common:1; Rare:42 | ||||
| chr3:42804252-42804310 | Rare:14 | ||||
| chr3:42804440-42804651 | Common:2; Rare:62 | ||||
| chr3:43286431-43286633 | Common:2; Rare:90 | ||||
| chr3:43690826-43690993 | Common:3; Rare:91; Clinvar:7; Clinvar (benign):2 | ||||
| chr3:44338666-44338825 | Common:3; Rare:56 |