| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:123233096-123233504 | Common:2; Rare:138; Clinvar:1 | ||||
| chr12:123364816-123364989 | Common:3; Rare:63 | ||||
| chr12:123584325-123584693 | Common:7; Rare:132 | ||||
| chr12:123602022-123602174 | Common:3; Rare:56 | ||||
| chr12:123633607-123633862 | Common:1; Rare:125; Clinvar:8; Clinvar (benign):1 | ||||
| chr12:123972565-123972895 | Common:6; Rare:114 | ||||
| chr12:124388797-124388951 | Common:3; Rare:46 | ||||
| chr12:124518546-124518828 | Rare:69 | ||||
| chr12:124786498-124786786 | Common:3; Rare:78 | ||||
| chr12:128853402-128853618 | Common:1; Rare:59 | ||||
| chr12:130716247-130716543 | Rare:45 | ||||
| chr12:130871771-130872122 | Common:4; Rare:140 | ||||
| chr12:131710839-131711125 | Rare:71 | ||||
| chr12:132687311-132687689 | Common:4; Rare:141; Clinvar:5; Clinvar (benign):10; Clinvar (pathogenic):1 | ||||
| chr12:132710751-132711035 | Common:3; Rare:90 |