| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:121802928-121803155 | Common:1; Rare:59 | ||||
| chr12:121888641-121888863 | Common:2; Rare:73 | ||||
| chr12:122526907-122527262 | Common:3; Rare:112 | ||||
| chr12:122835144-122835529 | Common:1; Rare:67 | ||||
| chr12:122980571-122980815 | Common:1; Rare:84 | ||||
| chr12:123233087-123233497 | Common:2; Rare:140; Clinvar:1 | ||||
| chr12:123584336-123584577 | Common:5; Rare:59 | ||||
| chr12:123584737-123584811 | Common:1; Rare:22 | ||||
| chr12:123633597-123633845 | Common:1; Rare:120; Clinvar:8; Clinvar (benign):1 | ||||
| chr12:131929046-131929306 | Common:10; Rare:80; Clinvar:1 | ||||
| chr12:132144310-132144489 | Rare:73 | ||||
| chr12:132687322-132687628 | Common:2; Rare:112; Clinvar:2; Clinvar (benign):8 | ||||
| chr13:19863517-19863823 | Common:5; Rare:108 | ||||
| chr13:21176487-21176696 | Common:2; Rare:92 | ||||
| chr13:24512723-24512897 | Common:3; Rare:52 |