| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:103965704-103965941 | Common:2; Rare:55 | ||||
| chr12:104064439-104064548 | Rare:26 | ||||
| chr12:104138164-104138362 | Rare:46 | ||||
| chr12:104287234-104287275 | Rare:9 | ||||
| chr12:104958254-104958480 | Common:4; Rare:62 | ||||
| chr12:104986201-104986355 | Common:2; Rare:49 | ||||
| chr12:105107612-105107795 | Common:1; Rare:84 | ||||
| chr12:105236091-105236294 | Common:1; Rare:93 | ||||
| chr12:106357952-106358111 | Common:3; Rare:74 | ||||
| chr12:106774547-106774692 | Rare:45 | ||||
| chr12:107093536-107093669 | Rare:42 | ||||
| chr12:107685709-107685852 | Rare:49 | ||||
| chr12:108562394-108562658 | Common:8; Rare:110; Clinvar:2; Clinvar (benign):3 | ||||
| chr12:108731486-108731697 | Common:2; Rare:76 | ||||
| chr12:109052495-109052644 | Common:2; Rare:42 |