| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:36993190-36993546 | Common:2; Rare:105; Clinvar:26; Clinvar (benign):10; Clinvar (pathogenic):1 | ||||
| chr3:37242982-37243352 | Common:5; Rare:97 | ||||
| chr3:39051902-39052042 | Common:1; Rare:45 | ||||
| chr3:39107597-39107697 | Common:3; Rare:31 | ||||
| chr3:39153555-39153730 | Common:3; Rare:60 | ||||
| chr3:39406579-39406758 | Common:2; Rare:78 | ||||
| chr3:40309533-40309808 | Common:7; Rare:96 | ||||
| chr3:40457204-40457363 | Common:2; Rare:79 | ||||
| chr3:40524823-40524886 | Common:1; Rare:12 | ||||
| chr3:42581909-42582123 | Common:2; Rare:67 | ||||
| chr3:42590687-42590939 | Common:3; Rare:78 | ||||
| chr3:42600372-42600709 | Common:2; Rare:133 | ||||
| chr3:42804443-42804635 | Common:2; Rare:56 | ||||
| chr3:43621919-43622322 | Common:2; Rare:118; Clinvar:7; Clinvar (benign):1 | ||||
| chr3:43690823-43690939 | Common:1; Rare:47; Clinvar:5; Clinvar (benign):1 |