| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:109093617-109093903 | Common:2; Rare:64 | ||||
| chr12:109097961-109098295 | Common:5; Rare:102 | ||||
| chr12:109477287-109477679 | Common:3; Rare:103 | ||||
| chr12:109573403-109573863 | Common:5; Rare:155; Clinvar:8; Clinvar (benign):8; Clinvar (pathogenic):2 | ||||
| chr12:109880371-109880668 | Common:1; Rare:91 | ||||
| chr12:109900177-109900370 | Rare:68 | ||||
| chr12:109996217-109996436 | Common:2; Rare:63 | ||||
| chr12:110450253-110450417 | Common:2; Rare:62 | ||||
| chr12:110468673-110468909 | Rare:58 | ||||
| chr12:110502060-110502324 | Common:1; Rare:94 | ||||
| chr12:111685724-111686134 | Rare:147 | ||||
| chr12:111841887-111841998 | Common:2; Rare:36 | ||||
| chr12:112013135-112013492 | Common:1; Rare:130 | ||||
| chr12:112108735-112108918 | Common:1; Rare:50 | ||||
| chr12:112906868-112906995 | Rare:23 |