| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:3753107-3753245 | Rare:36 | ||||
| chr12:4320949-4321266 | Common:5; Rare:122 | ||||
| chr12:4538497-4538927 | Common:3; Rare:93 | ||||
| chr12:4649019-4649144 | Common:2; Rare:40; Clinvar (benign):1 | ||||
| chr12:6200046-6200512 | Common:4; Rare:136 | ||||
| chr12:6383988-6384225 | Common:1; Rare:54 | ||||
| chr12:6493230-6493502 | Common:7; Rare:81 | ||||
| chr12:6493746-6494153 | Common:2; Rare:120 | ||||
| chr12:6568234-6568651 | Common:1; Rare:130 | ||||
| chr12:6723970-6724151 | Rare:44 | ||||
| chr12:6724168-6724303 | Common:1; Rare:31 | ||||
| chr12:6867318-6867555 | Common:2; Rare:96; Clinvar:1; Clinvar (benign):2 | ||||
| chr12:6873334-6873541 | Common:1; Rare:55 | ||||
| chr12:6970612-6970948 | Common:3; Rare:103 | ||||
| chr12:7189563-7189715 | Rare:56; Clinvar:3 |