| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:101280027-101280157 | Common:1; Rare:41 | ||||
| chr12:101407678-101408092 | Common:3; Rare:105 | ||||
| chr12:101666026-101666386 | Common:1; Rare:57 | ||||
| chr12:101666612-101666695 | Rare:18 | ||||
| chr12:101830583-101831058 | Common:6; Rare:186; Clinvar:3; Clinvar (benign):5; Clinvar (pathogenic):2 | ||||
| chr12:102120065-102120266 | Rare:82 | ||||
| chr12:102197813-102197870 | Rare:9 | ||||
| chr12:102480399-102480450 | Rare:10 | ||||
| chr12:102480452-102480565 | Rare:16 | ||||
| chr12:102958257-102958569 | Common:5; Rare:123; Clinvar (benign):2 | ||||
| chr12:103930033-103930561 | Common:9; Rare:178 | ||||
| chr12:103943569-103943868 | Rare:57 | ||||
| chr12:103956734-103956775 | Rare:13 | ||||
| chr12:103956955-103957275 | Common:4; Rare:78 | ||||
| chr12:103965614-103965941 | Common:2; Rare:88 |