| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:118135960-118136178 | Common:2; Rare:65 | ||||
| chr12:120201081-120201360 | Common:2; Rare:89 | ||||
| chr12:120446370-120446470 | Common:1; Rare:45 | ||||
| chr12:120469624-120469873 | Common:2; Rare:89 | ||||
| chr12:120495915-120496152 | Common:5; Rare:67 | ||||
| chr12:122526916-122527281 | Common:3; Rare:114 | ||||
| chr12:123233096-123233486 | Common:2; Rare:126; Clinvar:1 | ||||
| chr12:123364831-123364952 | Common:1; Rare:47 | ||||
| chr12:123584336-123584616 | Common:5; Rare:97 | ||||
| chr12:123633620-123633845 | Common:1; Rare:105; Clinvar:8; Clinvar (benign):1 | ||||
| chr13:19633487-19633727 | Common:1; Rare:92 | ||||
| chr13:21176473-21176708 | Common:2; Rare:103 | ||||
| chr13:24512739-24512838 | Common:3; Rare:30 | ||||
| chr13:24922795-24923115 | Common:2; Rare:109; Clinvar:1 | ||||
| chr13:25287436-25287635 | Common:3; Rare:68 |