| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:126405302-126405611 | Common:2; Rare:54 | ||||
| chr11:129815680-129815891 | Common:1; Rare:54 | ||||
| chr11:130069624-130069940 | Common:2; Rare:114 | ||||
| chr11:134253298-134253580 | Common:2; Rare:93; Clinvar (benign):1 | ||||
| chr12:389256-389340 | Rare:31 | ||||
| chr12:643624-643918 | Common:2; Rare:61 | ||||
| chr12:991109-991289 | Common:2; Rare:81 | ||||
| chr12:2877022-2877262 | Rare:71 | ||||
| chr12:4320949-4321253 | Common:5; Rare:115 | ||||
| chr12:4538455-4538927 | Common:3; Rare:106 | ||||
| chr12:4649016-4649158 | Common:2; Rare:51; Clinvar (benign):2 | ||||
| chr12:6375432-6375535 | Common:1; Rare:18; Clinvar:1; Clinvar (benign):2 | ||||
| chr12:6493244-6493374 | Common:5; Rare:35 | ||||
| chr12:6493746-6494141 | Common:2; Rare:116 | ||||
| chr12:6851236-6851472 | Rare:56 |