| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:111841847-111842241 | Common:3; Rare:111 | ||||
| chr12:112013129-112013475 | Common:1; Rare:122 | ||||
| chr12:113185422-113185769 | Common:9; Rare:133 | ||||
| chr12:113221038-113221319 | Common:2; Rare:80 | ||||
| chr12:114404184-114404505 | Common:5; Rare:68 | ||||
| chr12:114405776-114405883 | Common:1; Rare:18 | ||||
| chr12:114407992-114408208 | Common:1; Rare:38; Clinvar (benign):2 | ||||
| chr12:114408610-114409002 | Rare:83 | ||||
| chr12:118135971-118136211 | Common:2; Rare:70 | ||||
| chr12:118372846-118373192 | Common:2; Rare:93 | ||||
| chr12:119178663-119179093 | Common:1; Rare:74; Clinvar:2; Clinvar (benign):1 | ||||
| chr12:119179173-119179679 | Rare:154; Clinvar:10; Clinvar (benign):4 | ||||
| chr12:120064383-120064658 | Common:1; Rare:40 | ||||
| chr12:120116747-120116935 | Common:2; Rare:62 | ||||
| chr12:120201085-120201354 | Common:2; Rare:86 |