| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:14947160-14947569 | Common:5; Rare:172 | ||||
| chr3:14948363-14948681 | Common:2; Rare:99 | ||||
| chr3:15065187-15065402 | Common:2; Rare:83 | ||||
| chr3:15099122-15099489 | Rare:85 | ||||
| chr3:15206057-15206264 | Rare:79 | ||||
| chr3:15427440-15427786 | Common:2; Rare:112 | ||||
| chr3:15601512-15602033 | Common:6; Rare:237; Clinvar:7; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr3:15859782-15860176 | Common:5; Rare:119 | ||||
| chr3:16264827-16265243 | Common:2; Rare:143 | ||||
| chr3:17742509-17742952 | Common:4; Rare:156 | ||||
| chr3:19148169-19148604 | Common:3; Rare:108 | ||||
| chr3:19946974-19947491 | Common:7; Rare:189 | ||||
| chr3:19947494-19947778 | Common:3; Rare:81 | ||||
| chr3:20186176-20186377 | Common:1; Rare:56 | ||||
| chr3:21751147-21751428 | Common:3; Rare:87 |