| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:98645007-98645290 | Common:2; Rare:86 | ||||
| chr12:102120069-102120217 | Rare:56 | ||||
| chr12:103930098-103930511 | Common:8; Rare:144 | ||||
| chr12:103965705-103965941 | Common:2; Rare:55 | ||||
| chr12:105107612-105107785 | Common:1; Rare:78 | ||||
| chr12:108562399-108562649 | Common:5; Rare:101; Clinvar:2; Clinvar (benign):1 | ||||
| chr12:109097849-109098214 | Common:5; Rare:115 | ||||
| chr12:109573488-109573837 | Common:3; Rare:96; Clinvar:4; Clinvar (benign):3 | ||||
| chr12:109900207-109900306 | Rare:44 | ||||
| chr12:110450270-110450443 | Common:2; Rare:61 | ||||
| chr12:112013140-112013460 | Common:1; Rare:111 | ||||
| chr12:112938425-112938527 | Common:2; Rare:22 | ||||
| chr12:113185437-113185769 | Common:8; Rare:120 | ||||
| chr12:118135960-118136175 | Common:2; Rare:65 | ||||
| chr12:120194697-120194803 | Rare:40 |