| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:105107633-105107795 | Common:1; Rare:75 | ||||
| chr12:105236085-105236294 | Common:2; Rare:96 | ||||
| chr12:106774342-106774646 | Common:1; Rare:76 | ||||
| chr12:107685717-107685934 | Rare:71 | ||||
| chr12:108515005-108515319 | Common:1; Rare:94 | ||||
| chr12:109130759-109131035 | Common:2; Rare:47 | ||||
| chr12:109477280-109477656 | Common:3; Rare:94 | ||||
| chr12:109573432-109573813 | Common:3; Rare:125; Clinvar:5; Clinvar (benign):5; Clinvar (pathogenic):2 | ||||
| chr12:109880381-109880662 | Common:1; Rare:86 | ||||
| chr12:110502058-110502227 | Common:1; Rare:61 | ||||
| chr12:110613997-110614178 | Rare:54; Clinvar:2; Clinvar (benign):2 | ||||
| chr12:111369025-111369278 | Common:1; Rare:69 | ||||
| chr12:111685733-111686110 | Rare:137 | ||||
| chr12:111766743-111766977 | Rare:64 | ||||
| chr12:111841898-111842039 | Common:2; Rare:41 |