| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:4649010-4649178 | Common:2; Rare:57; Clinvar (benign):2 | ||||
| chr12:5968127-5968198 | Rare:25; Clinvar:2 | ||||
| chr12:6124407-6124467 | Rare:11 | ||||
| chr12:6200003-6200525 | Common:4; Rare:155 | ||||
| chr12:6341703-6342127 | Common:2; Rare:97; Clinvar:2; Clinvar (benign):4 | ||||
| chr12:6355270-6355573 | Common:1; Rare:86; Clinvar:3; Clinvar (benign):2 | ||||
| chr12:6374689-6375672 | Common:8; Rare:282; Clinvar:5; Clinvar (benign):9 | ||||
| chr12:6376021-6376471 | Common:3; Rare:83 | ||||
| chr12:6383988-6384293 | Common:2; Rare:69 | ||||
| chr12:6384777-6385103 | Common:2; Rare:68 | ||||
| chr12:6388345-6388408 | Rare:16 | ||||
| chr12:6444838-6444987 | Rare:26 | ||||
| chr12:6493064-6493386 | Common:7; Rare:94 | ||||
| chr12:6493755-6494126 | Common:2; Rare:108 | ||||
| chr12:6534290-6534578 | Common:5; Rare:121 |