| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:113185447-113185730 | Common:7; Rare:105 | ||||
| chr12:118016555-118016780 | Common:2; Rare:45 | ||||
| chr12:118061066-118061289 | Common:1; Rare:64 | ||||
| chr12:118135953-118136166 | Common:2; Rare:65 | ||||
| chr12:120201085-120201366 | Common:2; Rare:88 | ||||
| chr12:120438012-120438205 | Rare:85; Clinvar (benign):2 | ||||
| chr12:120446358-120446474 | Common:1; Rare:51 | ||||
| chr12:120495847-120496148 | Common:5; Rare:97 | ||||
| chr12:120529137-120529188 | Common:1; Rare:14 | ||||
| chr12:120581360-120581577 | Common:1; Rare:77 | ||||
| chr12:122526916-122527284 | Common:3; Rare:115 | ||||
| chr12:122752555-122752903 | Common:1; Rare:123 | ||||
| chr12:122980570-122980735 | Common:1; Rare:53 | ||||
| chr12:123233087-123233486 | Common:2; Rare:130; Clinvar:1 | ||||
| chr12:123364820-123364949 | Common:1; Rare:50 |