| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:100267047-100267461 | Common:3; Rare:168 | ||||
| chr12:100573413-100573768 | Rare:97 | ||||
| chr12:101407668-101408076 | Common:3; Rare:102 | ||||
| chr12:101697495-101697679 | Common:2; Rare:56 | ||||
| chr12:102120065-102120286 | Common:1; Rare:87 | ||||
| chr12:102480444-102480584 | Rare:18 | ||||
| chr12:102852726-102852863 | Rare:51; Clinvar:4; Clinvar (benign):2; Clinvar (pathogenic):21 | ||||
| chr12:102915206-102915345 | Common:2; Rare:17 | ||||
| chr12:102917074-102917392 | Common:4; Rare:101; Clinvar:2; Clinvar (benign):3; Clinvar (pathogenic):4 | ||||
| chr12:103587082-103587307 | Common:2; Rare:54 | ||||
| chr12:103841060-103841355 | Common:3; Rare:92 | ||||
| chr12:103930085-103930571 | Common:8; Rare:165 | ||||
| chr12:103965662-103965986 | Common:2; Rare:78 | ||||
| chr12:104138157-104138354 | Rare:43 | ||||
| chr12:104287216-104287324 | Rare:27 |