| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:128693150-128693317 | Common:1; Rare:46 | ||||
| chr11:128693391-128694266 | Common:7; Rare:195 | ||||
| chr11:134253314-134253586 | Common:2; Rare:87; Clinvar (benign):1 | ||||
| chr12:991111-991248 | Common:1; Rare:51 | ||||
| chr12:2877045-2877260 | Rare:64 | ||||
| chr12:4538444-4538780 | Rare:71 | ||||
| chr12:6451787-6452108 | Common:4; Rare:57 | ||||
| chr12:6493230-6493386 | Common:6; Rare:44 | ||||
| chr12:6534591-6534859 | Common:3; Rare:108 | ||||
| chr12:6568251-6568382 | Rare:49 | ||||
| chr12:6591482-6591697 | Rare:54 | ||||
| chr12:6752934-6753205 | Common:6; Rare:86 | ||||
| chr12:6970591-6971070 | Common:9; Rare:149; Clinvar (benign):2 | ||||
| chr12:7108475-7108671 | Common:1; Rare:58 | ||||
| chr12:11171607-11171631 | Rare:6 |