| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:129895502-129895651 | Common:1; Rare:62 | ||||
| chr11:130140147-130140486 | Common:1; Rare:82 | ||||
| chr11:130314403-130314495 | Common:1; Rare:27 | ||||
| chr11:130448401-130448668 | Rare:64 | ||||
| chr11:131909672-131909929 | Common:1; Rare:44 | ||||
| chr11:131911340-131911634 | Common:2; Rare:102 | ||||
| chr11:132310026-132310174 | Common:2; Rare:51 | ||||
| chr11:134223897-134224111 | Common:2; Rare:76 | ||||
| chr11:134224533-134224713 | Rare:68 | ||||
| chr11:134253278-134253655 | Common:3; Rare:144; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr12:389239-389386 | Rare:56 | ||||
| chr12:401420-401664 | Common:2; Rare:70 | ||||
| chr12:752351-752598 | Common:1; Rare:74 | ||||
| chr12:990425-990583 | Common:1; Rare:41 | ||||
| chr12:991100-991251 | Common:1; Rare:57 |