| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:109573443-109573813 | Common:3; Rare:120; Clinvar:4; Clinvar (benign):5; Clinvar (pathogenic):2 | ||||
| chr12:109880316-109880652 | Common:1; Rare:107 | ||||
| chr12:109900177-109900356 | Rare:64 | ||||
| chr12:110280487-110280711 | Rare:57 | ||||
| chr12:110281024-110281193 | Rare:66 | ||||
| chr12:110468713-110468909 | Rare:52 | ||||
| chr12:110502051-110502218 | Common:1; Rare:60 | ||||
| chr12:110920497-110920798 | Rare:85; Clinvar:1; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr12:111369002-111369208 | Common:1; Rare:55 | ||||
| chr12:111685769-111686110 | Rare:127 | ||||
| chr12:111841845-111841977 | Common:1; Rare:43 | ||||
| chr12:112013129-112013468 | Common:1; Rare:119 | ||||
| chr12:112409567-112409707 | Common:1; Rare:46 | ||||
| chr12:113165646-113165952 | Rare:112 | ||||
| chr12:113185429-113185769 | Common:9; Rare:127 |