| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:120495871-120496228 | Common:7; Rare:119 | ||||
| chr12:121210059-121210152 | Common:2; Rare:33 | ||||
| chr12:121399904-121400160 | Common:5; Rare:95 | ||||
| chr12:121802940-121803069 | Rare:31 | ||||
| chr12:122266404-122266553 | Common:2; Rare:60 | ||||
| chr12:122526911-122527291 | Common:3; Rare:125 | ||||
| chr12:122872017-122872228 | Rare:34 | ||||
| chr12:122980571-122980816 | Common:1; Rare:85 | ||||
| chr12:123233093-123233490 | Common:2; Rare:132; Clinvar:1 | ||||
| chr12:123364820-123364988 | Common:3; Rare:62 | ||||
| chr12:123584361-123584609 | Common:5; Rare:88 | ||||
| chr12:123633620-123633851 | Common:1; Rare:108; Clinvar:8; Clinvar (benign):1 | ||||
| chr12:123972985-123973303 | Common:2; Rare:100 | ||||
| chr12:124518546-124518759 | Rare:51 | ||||
| chr12:132687387-132687720 | Common:4; Rare:114 |