| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:103965677-103965906 | Common:2; Rare:68 | ||||
| chr12:104064345-104064545 | Common:1; Rare:45 | ||||
| chr12:104138170-104138379 | Common:1; Rare:53 | ||||
| chr12:105107619-105107785 | Common:1; Rare:76 | ||||
| chr12:107093514-107093623 | Rare:43 | ||||
| chr12:108339299-108339541 | Common:2; Rare:62 | ||||
| chr12:109097922-109098194 | Common:4; Rare:83 | ||||
| chr12:109477295-109477638 | Common:3; Rare:78 | ||||
| chr12:109573488-109573813 | Common:3; Rare:91; Clinvar:3; Clinvar (benign):3 | ||||
| chr12:109996309-109996434 | Common:2; Rare:33 | ||||
| chr12:110468667-110468907 | Rare:60 | ||||
| chr12:111841895-111842241 | Common:3; Rare:95 | ||||
| chr12:112013129-112013468 | Common:1; Rare:119 | ||||
| chr12:113185437-113185775 | Common:8; Rare:121 | ||||
| chr12:113335109-113335241 | Rare:43 |