| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:123633624-123633851 | Common:1; Rare:104; Clinvar:8; Clinvar (benign):1 | ||||
| chr12:123972580-123972667 | Common:3; Rare:29 | ||||
| chr12:123972989-123973314 | Common:2; Rare:104 | ||||
| chr12:124388797-124388978 | Common:3; Rare:53 | ||||
| chr12:124422614-124422955 | Common:4; Rare:87 | ||||
| chr12:124518538-124518759 | Rare:54 | ||||
| chr12:128824038-128824097 | Rare:20 | ||||
| chr12:130871771-130872110 | Common:4; Rare:135 | ||||
| chr12:131710795-131711107 | Rare:82 | ||||
| chr12:132687311-132687713 | Common:4; Rare:149; Clinvar:5; Clinvar (benign):10; Clinvar (pathogenic):1 | ||||
| chr12:132887553-132887861 | Rare:92 | ||||
| chr12:132956252-132956410 | Common:1; Rare:36 | ||||
| chr12:132986236-132986428 | Rare:40 | ||||
| chr12:133080694-133080975 | Common:2; Rare:92 | ||||
| chr12:133130238-133130652 | Common:7; Rare:137 |