| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:101830674-101830994 | Common:6; Rare:190; Clinvar:1; Clinvar (benign):5 | ||||
| chr12:101830920-101831214 | Rare:67 | ||||
| chr12:101877000-101877340 | Common:12; Rare:105 | ||||
| chr12:101877378-101877829 | Common:14; Rare:279 | ||||
| chr12:101908338-101908803 | Common:3; Rare:184 | ||||
| chr12:102061500-102061710 | Common:2; Rare:38 | ||||
| chr12:102061882-102062184 | Common:2; Rare:202 | ||||
| chr12:102119984-102120405 | Common:2; Rare:344 | ||||
| chr12:102917162-102917500 | Common:11; Rare:157; Clinvar:2; Clinvar (benign):6 | ||||
| chr12:102957315-102957713 | Common:4; Rare:93 | ||||
| chr12:102958240-102958930 | Common:11; Rare:363; Clinvar (benign):5 | ||||
| chr12:103496310-103496609 | Rare:54 | ||||
| chr12:103840690-103841070 | Common:1; Rare:99 | ||||
| chr12:103841118-103841509 | Common:14; Rare:348 | ||||
| chr12:103929990-103930565 | Common:25; Rare:490 |