| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:110450260-110450412 | Common:2; Rare:55 | ||||
| chr12:110468665-110468909 | Rare:62 | ||||
| chr12:110502058-110502332 | Common:1; Rare:100 | ||||
| chr12:110613997-110614187 | Rare:55; Clinvar:2; Clinvar (benign):2 | ||||
| chr12:111685827-111686116 | Rare:107 | ||||
| chr12:111766814-111766992 | Rare:58 | ||||
| chr12:111841894-111842010 | Common:2; Rare:38 | ||||
| chr12:112013129-112013466 | Common:1; Rare:119 | ||||
| chr12:112108738-112108860 | Common:1; Rare:37 | ||||
| chr12:112125371-112125570 | Rare:51 | ||||
| chr12:112907060-112907154 | Rare:30 | ||||
| chr12:113185447-113185783 | Common:8; Rare:115 | ||||
| chr12:113221088-113221319 | Common:1; Rare:73 | ||||
| chr12:113966279-113966562 | Common:10; Rare:92 | ||||
| chr12:118135938-118136179 | Common:2; Rare:76 |