| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:33798990-33799049 | Rare:22 | ||||
| chr3:36380364-36380674 | Common:4; Rare:110 | ||||
| chr3:36993036-36993607 | Common:2; Rare:203; Clinvar:39; Clinvar (benign):18; Clinvar (pathogenic):4 | ||||
| chr3:36993714-36993842 | Rare:50; Clinvar:1 | ||||
| chr3:37065808-37066058 | Common:2; Rare:61 | ||||
| chr3:37066266-37066413 | Common:1; Rare:48 | ||||
| chr3:37176022-37176397 | Common:1; Rare:106 | ||||
| chr3:37243178-37243603 | Common:1; Rare:120 | ||||
| chr3:37994076-37994177 | Rare:27 | ||||
| chr3:37999011-37999277 | Common:3; Rare:73 | ||||
| chr3:38008139-38008335 | Rare:69 | ||||
| chr3:38024436-38024668 | Common:1; Rare:88 | ||||
| chr3:38029572-38029864 | Common:2; Rare:59 | ||||
| chr3:38039163-38039540 | Common:1; Rare:139 | ||||
| chr3:38126631-38126807 | Common:1; Rare:40 |