| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:109477279-109477656 | Common:3; Rare:94 | ||||
| chr12:109573472-109573813 | Common:3; Rare:102; Clinvar:4; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr12:109880353-109880668 | Common:1; Rare:95 | ||||
| chr12:109899957-109900356 | Common:1; Rare:103 | ||||
| chr12:109996299-109996439 | Common:2; Rare:39 | ||||
| chr12:109999118-109999219 | Rare:16 | ||||
| chr12:110450264-110450443 | Common:2; Rare:63 | ||||
| chr12:110468671-110468938 | Rare:72 | ||||
| chr12:110502047-110502343 | Common:1; Rare:110 | ||||
| chr12:110613997-110614185 | Rare:55; Clinvar:2; Clinvar (benign):2 | ||||
| chr12:110742825-110743207 | Common:3; Rare:140 | ||||
| chr12:111685844-111686085 | Rare:91 | ||||
| chr12:111841867-111842230 | Common:3; Rare:99 | ||||
| chr12:112013134-112013463 | Common:1; Rare:114 | ||||
| chr12:112108741-112108862 | Common:1; Rare:35 |