| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:112409507-112409718 | Common:1; Rare:69 | ||||
| chr12:112418733-112419015 | Common:1; Rare:88; Clinvar:4; Clinvar (benign):1 | ||||
| chr12:112419106-112419357 | Common:2; Rare:58; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr12:112419362-112419575 | Rare:45 | ||||
| chr12:112906824-112907040 | Rare:47 | ||||
| chr12:112938311-112938608 | Common:4; Rare:70 | ||||
| chr12:113184708-113185149 | Common:2; Rare:112 | ||||
| chr12:113185367-113185856 | Common:10; Rare:181 | ||||
| chr12:113220958-113221581 | Common:5; Rare:167 | ||||
| chr12:113221610-113221750 | Rare:26 | ||||
| chr12:113221801-113221994 | Common:2; Rare:40 | ||||
| chr12:113335010-113335263 | Rare:68 | ||||
| chr12:113358332-113358651 | Common:2; Rare:113 | ||||
| chr12:113358976-113359099 | Common:2; Rare:22 | ||||
| chr12:113422305-113422436 | Common:2; Rare:35 |