| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:33277313-33277482 | Common:1; Rare:45 | ||||
| chr3:33798499-33798870 | Common:3; Rare:127 | ||||
| chr3:33798997-33799179 | Rare:59 | ||||
| chr3:36993073-36993573 | Common:2; Rare:173; Clinvar:29; Clinvar (benign):14; Clinvar (pathogenic):3 | ||||
| chr3:37176131-37176403 | Rare:77 | ||||
| chr3:37242913-37243388 | Common:6; Rare:127 | ||||
| chr3:38024470-38024643 | Common:1; Rare:66 | ||||
| chr3:38029612-38029864 | Common:1; Rare:51 | ||||
| chr3:38649534-38649896 | Common:4; Rare:108; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:39051956-39052038 | Common:1; Rare:31 | ||||
| chr3:39107562-39107725 | Common:3; Rare:51 | ||||
| chr3:39153496-39153771 | Common:4; Rare:93 | ||||
| chr3:39192451-39192662 | Rare:35 | ||||
| chr3:40309436-40309972 | Common:9; Rare:179 | ||||
| chr3:40457207-40457370 | Common:2; Rare:78 |