| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:100142847-100143104 | Common:3; Rare:89 | ||||
| chr12:100199708-100200074 | Common:2; Rare:80 | ||||
| chr12:100200695-100200869 | Rare:57 | ||||
| chr12:100266956-100267399 | Common:2; Rare:191 | ||||
| chr12:100573531-100573745 | Rare:74 | ||||
| chr12:101280025-101280231 | Common:1; Rare:56 | ||||
| chr12:101407652-101408035 | Common:3; Rare:95 | ||||
| chr12:101830642-101830980 | Common:6; Rare:144; Clinvar:1; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr12:101877489-101877643 | Common:1; Rare:38 | ||||
| chr12:102120025-102120263 | Rare:98 | ||||
| chr12:102917214-102917369 | Common:2; Rare:46; Clinvar (benign):1 | ||||
| chr12:103841192-103841471 | Common:5; Rare:105 | ||||
| chr12:103930282-103930582 | Common:7; Rare:116 | ||||
| chr12:103965658-103966012 | Common:3; Rare:89 | ||||
| chr12:104064435-104064556 | Rare:29 |