| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:38905569-38905792 | Common:5; Rare:59 | ||||
| chr12:39443105-39443451 | Common:2; Rare:103; Clinvar:8; Clinvar (benign):5 | ||||
| chr12:40692285-40692550 | Common:1; Rare:84 | ||||
| chr12:41437622-41437787 | Rare:34 | ||||
| chr12:42326065-42326206 | Common:1; Rare:43 | ||||
| chr12:43758745-43759007 | Common:2; Rare:73; Clinvar:2 | ||||
| chr12:43806241-43806385 | Common:2; Rare:50 | ||||
| chr12:44876042-44876459 | Common:3; Rare:131 | ||||
| chr12:45216011-45216163 | Rare:48 | ||||
| chr12:45990543-45990917 | Common:2; Rare:119 | ||||
| chr12:46267324-46267409 | Rare:21 | ||||
| chr12:46268750-46269231 | Common:1; Rare:129 | ||||
| chr12:46269240-46269450 | Rare:51 | ||||
| chr12:46372664-46372915 | Rare:111 | ||||
| chr12:47705962-47706088 | Rare:57 |