| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:107093391-107094120 | Common:14; Rare:910 | ||||
| chr12:107685166-107685589 | Common:12; Rare:97 | ||||
| chr12:107685608-107686045 | Common:8; Rare:725 | ||||
| chr12:107760391-107760815 | Common:2; Rare:194 | ||||
| chr12:107761009-107761412 | Common:19; Rare:448 | ||||
| chr12:108128940-108129450 | Common:8; Rare:87 | ||||
| chr12:108129492-108129747 | Common:1; Rare:170 | ||||
| chr12:108129701-108130101 | Common:5; Rare:128 | ||||
| chr12:108514935-108515398 | Common:9; Rare:833 | ||||
| chr12:108515428-108515828 | Common:2; Rare:72 | ||||
| chr12:108532532-108532932 | Common:2; Rare:133 | ||||
| chr12:108560201-108561893 | Common:29; Rare:1035 | ||||
| chr12:108561912-108562312 | Common:9; Rare:61 | ||||
| chr12:108562239-108562731 | Common:52; Rare:839; Clinvar:12; Clinvar (benign):20 | ||||
| chr12:108562840-108563260 | Common:5; Rare:164 |