| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:123633582-123633878 | Common:4; Rare:281; Clinvar:16; Clinvar (benign):2 | ||||
| chr12:123712195-123712444 | Common:8; Rare:188; Clinvar:4; Clinvar (benign):4 | ||||
| chr12:123972828-123973353 | Common:5; Rare:256 | ||||
| chr12:124388797-124389104 | Common:7; Rare:147 | ||||
| chr12:124495190-124495610 | Common:10; Rare:228 | ||||
| chr12:124518280-124518390 | Common:2; Rare:26 | ||||
| chr12:124817420-124818001 | Common:5; Rare:284 | ||||
| chr12:124863682-124864081 | Common:5; Rare:184 | ||||
| chr12:124913950-124914360 | Common:10; Rare:178 | ||||
| chr12:124914567-124915180 | Common:12; Rare:368 | ||||
| chr12:124989009-124989268 | Common:8; Rare:145 | ||||
| chr12:124993468-124993773 | Common:1; Rare:156 | ||||
| chr12:125065276-125065476 | Common:4; Rare:145 | ||||
| chr12:128823910-128824141 | Common:6; Rare:155 | ||||
| chr12:130871679-130872124 | Common:8; Rare:358 |