| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:120495859-120496171 | Common:6; Rare:105 | ||||
| chr12:121209887-121210152 | Common:5; Rare:80 | ||||
| chr12:121399885-121400144 | Common:5; Rare:93 | ||||
| chr12:121888641-121888868 | Common:2; Rare:74 | ||||
| chr12:122526911-122527281 | Common:3; Rare:119 | ||||
| chr12:122979971-122980262 | Rare:76 | ||||
| chr12:122980552-122980950 | Common:2; Rare:115 | ||||
| chr12:123233087-123233506 | Common:2; Rare:142; Clinvar:1 | ||||
| chr12:123364808-123364969 | Common:2; Rare:64 | ||||
| chr12:123584387-123584639 | Common:2; Rare:102 | ||||
| chr12:123602031-123602138 | Common:3; Rare:34 | ||||
| chr12:123633624-123633856 | Common:1; Rare:107; Clinvar:8; Clinvar (benign):1 | ||||
| chr12:123973015-123973312 | Common:2; Rare:98 | ||||
| chr12:131710795-131711105 | Rare:81 | ||||
| chr12:132687368-132687726 | Common:4; Rare:121 |