| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:33096728-33096831 | Rare:31 | ||||
| chr3:33097048-33097334 | Common:5; Rare:92; Clinvar:4; Clinvar (benign):3 | ||||
| chr3:33097373-33097563 | Common:3; Rare:39 | ||||
| chr3:33113802-33114237 | Common:2; Rare:157; Clinvar:8; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr3:33114368-33114647 | Common:1; Rare:108; Clinvar:4; Clinvar (benign):4; Clinvar (pathogenic):2 | ||||
| chr3:33439758-33439808 | Rare:15 | ||||
| chr3:33440000-33440177 | Rare:58 | ||||
| chr3:33440305-33440489 | Common:1; Rare:54 | ||||
| chr3:33440781-33441180 | Common:2; Rare:92 | ||||
| chr3:33441201-33441351 | Rare:22 | ||||
| chr3:33717753-33717921 | Common:1; Rare:52 | ||||
| chr3:33718153-33718452 | Rare:121 | ||||
| chr3:33798448-33798748 | Common:2; Rare:102 | ||||
| chr3:33798875-33798934 | Rare:28 | ||||
| chr3:33798949-33799130 | Rare:56 |