| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:122422541-122422875 | Common:4; Rare:101 | ||||
| chr12:122500846-122501134 | Common:2; Rare:80 | ||||
| chr12:122526849-122527291 | Common:4; Rare:162 | ||||
| chr12:122752588-122752899 | Common:1; Rare:111 | ||||
| chr12:122834738-122834757 | Rare:4 | ||||
| chr12:122896058-122896226 | Rare:88 | ||||
| chr12:122975133-122975253 | Common:1; Rare:34 | ||||
| chr12:122980570-122980727 | Rare:51 | ||||
| chr12:123233087-123233501 | Common:2; Rare:142; Clinvar:1 | ||||
| chr12:123268178-123268329 | Rare:29 | ||||
| chr12:123364825-123364980 | Common:3; Rare:58 | ||||
| chr12:123458107-123458213 | Rare:27 | ||||
| chr12:123584317-123584609 | Common:6; Rare:97 | ||||
| chr12:123601814-123602156 | Common:6; Rare:90 | ||||
| chr12:123633624-123633851 | Common:1; Rare:104; Clinvar:8; Clinvar (benign):1 |