| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:121805869-121805975 | Rare:13 | ||||
| chr12:121812038-121812438 | Common:8; Rare:195 | ||||
| chr12:121812476-121812989 | Common:7; Rare:196 | ||||
| chr12:121839252-121839950 | Common:4; Rare:478; Clinvar:3 | ||||
| chr12:122020123-122021096 | Common:6; Rare:227 | ||||
| chr12:122023312-122023443 | Rare:26 | ||||
| chr12:122023419-122023672 | Common:1; Rare:61 | ||||
| chr12:122035153-122036169 | Common:8; Rare:402 | ||||
| chr12:122062980-122063620 | Common:4; Rare:186 | ||||
| chr12:122063966-122064366 | Common:6; Rare:128 | ||||
| chr12:122072450-122072990 | Common:3; Rare:87 | ||||
| chr12:122080398-122080798 | Common:4; Rare:135 | ||||
| chr12:122097820-122098430 | Common:6; Rare:216 | ||||
| chr12:122197008-122197219 | Common:1; Rare:32 | ||||
| chr12:122224214-122225447 | Common:8; Rare:648; Clinvar:2; Clinvar (benign):2 |