| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:32106378-32106697 | Common:4; Rare:88; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:32502787-32502938 | Rare:39 | ||||
| chr3:32570738-32570948 | Common:1; Rare:95 | ||||
| chr3:32685070-32685379 | Rare:94 | ||||
| chr3:33097087-33097285 | Common:2; Rare:66; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:33277283-33277487 | Common:2; Rare:55 | ||||
| chr3:33798499-33798868 | Common:3; Rare:126 | ||||
| chr3:36993098-36993559 | Common:2; Rare:150; Clinvar:26; Clinvar (benign):12; Clinvar (pathogenic):3 | ||||
| chr3:36993690-36993826 | Rare:56; Clinvar:1 | ||||
| chr3:37243158-37243365 | Common:1; Rare:52 | ||||
| chr3:37994093-37994160 | Rare:21 | ||||
| chr3:38024510-38024634 | Common:1; Rare:46 | ||||
| chr3:38029636-38029819 | Common:1; Rare:36 | ||||
| chr3:39051939-39052052 | Common:1; Rare:41 | ||||
| chr3:39107562-39107725 | Common:3; Rare:51 |