| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:38905580-38905664 | Common:3; Rare:25 | ||||
| chr12:38906501-38906567 | Rare:14 | ||||
| chr12:38906683-38906805 | Common:1; Rare:30 | ||||
| chr12:39442874-39443246 | Common:2; Rare:100; Clinvar:5; Clinvar (benign):5 | ||||
| chr12:39443258-39443509 | Common:1; Rare:79; Clinvar:4; Clinvar (benign):2 | ||||
| chr12:39619756-39620055 | Common:1; Rare:48 | ||||
| chr12:40692319-40692585 | Common:1; Rare:83 | ||||
| chr12:40827661-40828018 | Rare:63 | ||||
| chr12:40828106-40828209 | Rare:17 | ||||
| chr12:41437489-41437898 | Rare:83 | ||||
| chr12:42237462-42237536 | Rare:17 | ||||
| chr12:42238157-42238471 | Common:1; Rare:101 | ||||
| chr12:42325956-42326229 | Common:2; Rare:88 | ||||
| chr12:42589340-42589380 | Rare:9 | ||||
| chr12:43758535-43758993 | Common:10; Rare:124; Clinvar:2 |