| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:120446353-120446485 | Common:1; Rare:62 | ||||
| chr12:120469518-120469895 | Common:4; Rare:128 | ||||
| chr12:120495867-120496228 | Common:7; Rare:121 | ||||
| chr12:121209931-121210152 | Common:5; Rare:69 | ||||
| chr12:121399916-121400180 | Common:3; Rare:101 | ||||
| chr12:121802919-121803015 | Rare:25 | ||||
| chr12:122526864-122527260 | Common:4; Rare:136 | ||||
| chr12:122752703-122752944 | Common:1; Rare:86 | ||||
| chr12:122975200-122975252 | Rare:18 | ||||
| chr12:122980590-122980941 | Common:2; Rare:102 | ||||
| chr12:123233096-123233507 | Common:2; Rare:138; Clinvar:1 | ||||
| chr12:123364821-123364992 | Common:3; Rare:64 | ||||
| chr12:123533209-123533364 | Common:1; Rare:35 | ||||
| chr12:123584325-123584813 | Common:8; Rare:163 | ||||
| chr12:123633624-123633851 | Common:1; Rare:104; Clinvar:8; Clinvar (benign):1 |