| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:122980570-122980745 | Common:1; Rare:57 | ||||
| chr12:123233096-123233490 | Common:2; Rare:130; Clinvar:1 | ||||
| chr12:123364808-123364990 | Common:3; Rare:69 | ||||
| chr12:123436457-123436550 | Rare:11 | ||||
| chr12:123584360-123584753 | Common:7; Rare:140 | ||||
| chr12:123602016-123602156 | Common:3; Rare:47 | ||||
| chr12:123633624-123633851 | Common:1; Rare:104; Clinvar:8; Clinvar (benign):1 | ||||
| chr12:123972580-123972899 | Common:6; Rare:110 | ||||
| chr12:124913607-124914145 | Common:5; Rare:207 | ||||
| chr12:130871766-130872120 | Common:4; Rare:140 | ||||
| chr12:130953760-130953973 | Rare:39 | ||||
| chr12:131710788-131711113 | Rare:87 | ||||
| chr12:132144118-132144496 | Common:3; Rare:130 | ||||
| chr12:132687305-132687689 | Common:4; Rare:143; Clinvar:7; Clinvar (benign):10; Clinvar (pathogenic):1 | ||||
| chr12:132710758-132711042 | Common:3; Rare:89 |