| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:38029636-38029844 | Common:1; Rare:42 | ||||
| chr3:38164974-38165217 | Common:1; Rare:56 | ||||
| chr3:38496022-38496349 | Common:2; Rare:87 | ||||
| chr3:39051950-39052068 | Common:1; Rare:44 | ||||
| chr3:39107553-39107704 | Common:3; Rare:48 | ||||
| chr3:39383269-39383442 | Common:2; Rare:30; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:39383561-39383683 | Rare:31; Clinvar:2 | ||||
| chr3:39406574-39406758 | Common:2; Rare:79 | ||||
| chr3:40309460-40309894 | Common:9; Rare:142 | ||||
| chr3:40457201-40457413 | Common:3; Rare:105 | ||||
| chr3:40477081-40477179 | Common:1; Rare:25 | ||||
| chr3:40524815-40525013 | Common:1; Rare:58 | ||||
| chr3:41962040-41962371 | Common:4; Rare:81 | ||||
| chr3:42159848-42160239 | Common:1; Rare:74 | ||||
| chr3:42581895-42582132 | Common:3; Rare:73 |