| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:143971341-143971492 | Common:2; Rare:112 | ||||
| chr3:143971520-143971854 | Common:4; Rare:186 | ||||
| chr3:143971967-143972215 | Common:2; Rare:106 | ||||
| chr3:146160983-146161232 | Common:1; Rare:129; Clinvar:7; Clinvar (benign):3 | ||||
| chr3:146161154-146161267 | Common:1; Rare:30; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:146251010-146251430 | Common:4; Rare:161 | ||||
| chr3:146469220-146469700 | Common:10; Rare:206 | ||||
| chr3:146469690-146470050 | Common:12; Rare:144 | ||||
| chr3:146544484-146544824 | Common:8; Rare:138 | ||||
| chr3:148991245-148991577 | Common:7; Rare:188 | ||||
| chr3:149086455-149086733 | Rare:155 | ||||
| chr3:149129484-149129737 | Common:3; Rare:197; Clinvar:4; Clinvar (benign):2 | ||||
| chr3:149375220-149375710 | Common:2; Rare:169 | ||||
| chr3:149377013-149377340 | Rare:89 | ||||
| chr3:149377355-149377908 | Common:2; Rare:297 |