| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:109573423-109573813 | Common:4; Rare:132; Clinvar:6; Clinvar (benign):6; Clinvar (pathogenic):2 | ||||
| chr12:110346069-110346392 | Common:2; Rare:89; Clinvar (benign):3 | ||||
| chr12:110502058-110502226 | Common:1; Rare:60 | ||||
| chr12:111685761-111686127 | Rare:136 | ||||
| chr12:111766823-111766992 | Rare:55 | ||||
| chr12:111841877-111842033 | Common:2; Rare:46 | ||||
| chr12:112013129-112013468 | Common:1; Rare:119 | ||||
| chr12:112906831-112907042 | Rare:49 | ||||
| chr12:113185391-113185783 | Common:10; Rare:150 | ||||
| chr12:113966192-113966491 | Common:6; Rare:96 | ||||
| chr12:114684143-114684353 | Rare:55 | ||||
| chr12:118103886-118104128 | Common:1; Rare:57 | ||||
| chr12:118135941-118136226 | Common:2; Rare:92 | ||||
| chr12:118372868-118373192 | Common:1; Rare:85 | ||||
| chr12:118376448-118376739 | Common:1; Rare:94 |