| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:14947170-14947551 | Common:5; Rare:158 | ||||
| chr3:14948024-14948122 | Rare:49 | ||||
| chr3:15065072-15065360 | Common:2; Rare:106 | ||||
| chr3:15099122-15099299 | Rare:43 | ||||
| chr3:15206047-15206278 | Rare:88 | ||||
| chr3:15427471-15427635 | Common:1; Rare:60 | ||||
| chr3:15601462-15601810 | Common:4; Rare:144; Clinvar:2 | ||||
| chr3:15601853-15602046 | Common:1; Rare:99; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr3:15859761-15860127 | Common:4; Rare:122 | ||||
| chr3:16264830-16265243 | Common:2; Rare:142 | ||||
| chr3:17742591-17742952 | Common:4; Rare:127 | ||||
| chr3:18425312-18425561 | Common:3; Rare:78 | ||||
| chr3:19946974-19947450 | Common:7; Rare:177 | ||||
| chr3:20147795-20147994 | Common:2; Rare:34 | ||||
| chr3:20186133-20186416 | Common:4; Rare:92 |