| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:111842687-111842749 | Rare:16 | ||||
| chr12:112006027-112006286 | Common:4; Rare:41 | ||||
| chr12:112013102-112013595 | Common:1; Rare:188 | ||||
| chr12:112477696-112477955 | Rare:52; Clinvar:3; Clinvar (benign):8; Clinvar (pathogenic):3 | ||||
| chr12:112906811-112907021 | Common:1; Rare:40 | ||||
| chr12:113161776-113162000 | Common:1; Rare:55 | ||||
| chr12:113185320-113185777 | Common:10; Rare:182 | ||||
| chr12:113185883-113185980 | Common:1; Rare:22 | ||||
| chr12:113221000-113221489 | Common:4; Rare:134 | ||||
| chr12:113422112-113422436 | Common:3; Rare:69 | ||||
| chr12:116738028-116738353 | Common:4; Rare:102 | ||||
| chr12:116910851-116911055 | Rare:66 | ||||
| chr12:117099351-117099532 | Common:1; Rare:61 | ||||
| chr12:117190218-117190346 | Rare:37 | ||||
| chr12:118016559-118016827 | Common:2; Rare:57 |