| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:98593505-98593958 | Common:1; Rare:138; Clinvar:4; Clinvar (benign):5 | ||||
| chr12:98644992-98645293 | Common:2; Rare:90 | ||||
| chr12:100200710-100200846 | Rare:41 | ||||
| chr12:100267065-100267403 | Common:1; Rare:137 | ||||
| chr12:101407641-101408061 | Common:3; Rare:107 | ||||
| chr12:101877437-101877734 | Common:3; Rare:77 | ||||
| chr12:102120065-102120247 | Rare:69 | ||||
| chr12:102478536-102478834 | Common:1; Rare:57 | ||||
| chr12:103793409-103793609 | Rare:48 | ||||
| chr12:103793913-103794283 | Common:8; Rare:69 | ||||
| chr12:103841008-103841468 | Common:6; Rare:139 | ||||
| chr12:103929980-103930329 | Common:5; Rare:87 | ||||
| chr12:103930332-103930564 | Common:4; Rare:102 | ||||
| chr12:103965701-103965941 | Common:2; Rare:56 | ||||
| chr12:104064113-104064120 | Rare:3 |