| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:186784131-186784477 | Common:1; Rare:139 | ||||
| chr3:186806393-186806575 | Rare:62 | ||||
| chr3:186930430-186930771 | Common:2; Rare:88 | ||||
| chr3:187139436-187139564 | Rare:49 | ||||
| chr3:187291679-187291834 | Common:1; Rare:56 | ||||
| chr3:187737724-187738139 | Common:3; Rare:60 | ||||
| chr3:188152892-188153038 | Common:1; Rare:22 | ||||
| chr3:188153756-188154230 | Common:1; Rare:115 | ||||
| chr3:188584304-188584414 | Common:2; Rare:19 | ||||
| chr3:188947404-188947716 | Rare:73 | ||||
| chr3:190120309-190120688 | Common:1; Rare:160; Clinvar (pathogenic):1 | ||||
| chr3:190120834-190120996 | Rare:49 | ||||
| chr3:190322213-190322552 | Common:3; Rare:89; Clinvar (benign):1 | ||||
| chr3:190323025-190323224 | Common:3; Rare:41 | ||||
| chr3:190513860-190514145 | Common:2; Rare:79 |