| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:27710738-27710853 | Common:1; Rare:45 | ||||
| chr12:28190367-28190506 | Common:1; Rare:44 | ||||
| chr12:30695827-30696002 | Common:2; Rare:45 | ||||
| chr12:30754893-30755168 | Common:3; Rare:107 | ||||
| chr12:31073716-31073902 | Common:8; Rare:65 | ||||
| chr12:31326083-31326441 | Common:4; Rare:124 | ||||
| chr12:31729004-31729288 | Common:1; Rare:86 | ||||
| chr12:31959271-31959487 | Common:2; Rare:70 | ||||
| chr12:32755878-32756021 | Rare:47 | ||||
| chr12:32896744-32897043 | Common:4; Rare:94; Clinvar:4; Clinvar (benign):5 | ||||
| chr12:38905506-38905702 | Common:3; Rare:53 | ||||
| chr12:38906269-38906399 | Common:1; Rare:32 | ||||
| chr12:40225460-40225580 | Common:1; Rare:26; Clinvar:1 | ||||
| chr12:42238176-42238496 | Common:4; Rare:109 | ||||
| chr12:42325923-42326061 | Rare:39 |