| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:120469554-120469901 | Common:3; Rare:121 | ||||
| chr12:120495900-120496216 | Common:6; Rare:104 | ||||
| chr12:122266404-122266553 | Common:2; Rare:60 | ||||
| chr12:122526916-122527291 | Common:3; Rare:120 | ||||
| chr12:123233096-123233486 | Common:2; Rare:126; Clinvar:1 | ||||
| chr12:123364825-123364972 | Common:2; Rare:58 | ||||
| chr12:123584336-123584614 | Common:5; Rare:96 | ||||
| chr12:123601976-123602139 | Common:4; Rare:49 | ||||
| chr12:123633624-123633851 | Common:1; Rare:104; Clinvar:8; Clinvar (benign):1 | ||||
| chr12:131710834-131711107 | Rare:65 | ||||
| chr12:132687311-132687679 | Common:4; Rare:136; Clinvar:5; Clinvar (benign):10; Clinvar (pathogenic):1 | ||||
| chr12:132887558-132887845 | Rare:82 | ||||
| chr13:19181790-19182052 | Common:12; Rare:96 | ||||
| chr13:21140439-21140609 | Rare:92 | ||||
| chr13:21176478-21176704 | Common:2; Rare:99 |