| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:120495845-120496216 | Common:7; Rare:127 | ||||
| chr12:120581358-120581588 | Common:1; Rare:81 | ||||
| chr12:121802940-121803091 | Rare:35 | ||||
| chr12:122526911-122527301 | Common:3; Rare:127 | ||||
| chr12:122980570-122980956 | Common:2; Rare:110 | ||||
| chr12:123233087-123233490 | Common:2; Rare:134; Clinvar:1 | ||||
| chr12:123364816-123364972 | Common:2; Rare:61 | ||||
| chr12:123584284-123584645 | Common:6; Rare:127 | ||||
| chr12:123602023-123602139 | Common:3; Rare:37 | ||||
| chr12:123633624-123633856 | Common:1; Rare:107; Clinvar:8; Clinvar (benign):1 | ||||
| chr12:123972565-123972929 | Common:6; Rare:122 | ||||
| chr12:124422642-124422808 | Common:2; Rare:44 | ||||
| chr12:130871694-130872126 | Common:4; Rare:178 | ||||
| chr12:131710779-131711106 | Rare:89 | ||||
| chr12:132687322-132687470 | Rare:59; Clinvar:2; Clinvar (benign):8 |