| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:101796697-101796908 | Common:2; Rare:48; Clinvar:2; Clinvar (pathogenic):2 | ||||
| chr12:103946619-103946936 | Rare:79 | ||||
| chr12:105184136-105184276 | Common:1; Rare:22 | ||||
| chr12:106138787-106139098 | Rare:81 | ||||
| chr12:107864772-107864963 | Rare:30 | ||||
| chr12:108802323-108802428 | Rare:13 | ||||
| chr12:109111245-109111399 | Rare:30 | ||||
| chr12:109170362-109170446 | Rare:16 | ||||
| chr12:109209154-109209472 | Rare:89 | ||||
| chr12:109233796-109234053 | Common:2; Rare:87 | ||||
| chr12:116675379-116675633 | Common:3; Rare:51 | ||||
| chr12:124423100-124423340 | Common:2; Rare:67 | ||||
| chr12:124713150-124713334 | Common:1; Rare:43 | ||||
| chr12:127146001-127146235 | Rare:92 | ||||
| chr12:130875725-130875995 | Common:2; Rare:62 |