| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:42719496-42719633 | Common:1; Rare:24 | ||||
| chr3:42773187-42773529 | Common:1; Rare:83 | ||||
| chr3:42804407-42804697 | Common:2; Rare:95 | ||||
| chr3:42906087-42906354 | Common:4; Rare:78 | ||||
| chr3:42936071-42936455 | Common:2; Rare:95 | ||||
| chr3:43286449-43286654 | Common:2; Rare:91 | ||||
| chr3:43621919-43622175 | Common:2; Rare:91; Clinvar:7; Clinvar (benign):1 | ||||
| chr3:43690802-43691013 | Common:4; Rare:115; Clinvar:7; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr3:43691554-43691662 | Common:1; Rare:18 | ||||
| chr3:44241849-44242023 | Rare:57 | ||||
| chr3:44338057-44338200 | Common:2; Rare:49 | ||||
| chr3:44338331-44338809 | Common:8; Rare:158 | ||||
| chr3:44423974-44424136 | Rare:32 | ||||
| chr3:44477622-44477780 | Common:1; Rare:37 | ||||
| chr3:44510570-44510666 | Common:3; Rare:28 |