| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:146250350-146250710 | Rare:69 | ||||
| chr3:146251010-146251420 | Common:5; Rare:233 | ||||
| chr3:146543689-146544260 | Common:16; Rare:214 | ||||
| chr3:146544464-146544810 | Common:12; Rare:223 | ||||
| chr3:147392240-147392570 | Rare:235 | ||||
| chr3:147393349-147394186 | Common:4; Rare:341 | ||||
| chr3:147394350-147394536 | Common:2; Rare:39 | ||||
| chr3:148697963-148698105 | Common:1; Rare:35; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:148739567-148740565 | Common:24; Rare:283 | ||||
| chr3:148991312-148991662 | Common:12; Rare:284; Clinvar (benign):2 | ||||
| chr3:148992164-148992344 | Common:1; Rare:49 | ||||
| chr3:149086420-149086773 | Common:1; Rare:286 | ||||
| chr3:149129447-149129773 | Common:8; Rare:394; Clinvar:6; Clinvar (benign):3 | ||||
| chr3:149377600-149378210 | Common:4; Rare:260 | ||||
| chr3:149473600-149474120 | Common:15; Rare:130 |